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Haplogroup O-M176 | |
---|---|
Possible time of origin | 31,108 (95% CI 22,844 <-> 34,893) years before present[1] 29,190 years before present[2] 28,200 [95% CI 26,000 <-> 30,400] years before present[3] |
Coalescence age | 25,660 years before present[2] 25,800 [95% CI 23,400 <-> 28,400] years before present (YFull[3][4]) |
Possible place of origin | the Korean Peninsula or a nearby part of northeastern Asia[5] |
Ancestor | O-P31 |
Defining mutations | M176/SRY465, P49, 022454[citation needed] |
Highest frequencies | Japanese, Koreans, Ryukyuans, Manchus
|
Haplogroup O-M176 (aka O-SRY465) or O1b2 is a human Y-chromosome DNA haplogroup. It is best known for its part in the settlement of Korea and Japan. It is a descendant of Haplogroup O-P31, and it has been estimated to share a most recent common ancestor with its nearest outgroup, Haplogroup O-K18, approximately 31,108 (95% CI 22,844 <-> 34,893) years before present,[1] approximately 29,190 years before present,[2] or approximately 28,200 (95% CI 26,000 <-> 30,400) years before present.[3]
Distribution
editHaplogroup O-M176 is found mainly in the northernmost parts of East Asia, from the Uriankhai and Zakhchin peoples of western Mongolia (Katoh et al. 2005) to the Japanese of Japan, though it also has been detected sporadically in the Buryats (Jin et al. 2003). It has been detected with moderate frequencies in Udegeys (Jin, Kim & Kim 2010) of southern Siberia, rarely among populations of Southeast Asia including Indonesia (Hammer et al. 2006 and Jin et al. 2003), the Philippines (Jin et al. 2003), Thailand (Jin et al. 2003), and Vietnam (Hammer et al. 2006 and Jin et al. 2003), and Micronesians (Hammer et al. 2006). This haplogroup is found with its highest frequency and diversity values among modern populations of Japan and Korea and is rare in most populations in China. Among Han Chinese, it has been detected in some samples of Han Chinese from Beijing (1/51, Jin et al. 2003 and Kim et al. 2011),[5] Xi'an (1/34, Kim et al. 2011),[5] one Han Chinese in Henan,[19] Han Chinese in Taiwan (2/352 = 0.57%, including one of 34 Hakka people and one of 258 miscellaneous Han volunteers),[20] Han Chinese from East China sampled from the infertility clinic at the Affiliated Hospitals of Nanjing Medical University at Jiangsu (6/1147 = 0.52%, Lu et al. 2009), Wuhan (1/160),[21] and South China outside of Jiangsu, Anhui, Zhejiang, and Shanghai (1/65).[22] Among ethnic minorities in China, haplogroup O-M176 has been detected with high frequency in samples of Koreans in China (Xue et al. 2006 and Katoh et al. 2005) and with low frequency among Manchus[23] (Xue et al. 2006, Katoh et al. 2005, and Karafet et al. 2001), Hezhe people,[12] Daurs,[12] Evenks,[11] Sibes (Xue et al. 2006), Kham Tibetans,[24] and Hui.[25] In a study of various populations of Hunan, O1b2-M176 was found in 0.55% (5/903) of all samples; specifically, this haplogroup was observed in 3.0% (1/33) of a sample of Iu Mien from Hunan, 1.9% (2/103) of a sample of Gàn Chinese from Hunan, 1.4% (1/71) of a sample of Kam from Hunan, and 1.1% (1/95) of a sample of Xong Miao from Hunan.[26] In a study published in July 2020, Y-DNA belonging to haplogroup O1b2-M176 was observed in 1.31% (4/305) of a sample of Han Chinese from Zibo, Shandong and in 1.06% (6/565) of a sample of Han Chinese from Zhaotong, Yunnan.[27]
Mitsuru Sakitani suggests that haplogroup O1b2, which is common in today Koreans, Japanese and Manchu, are one of the carriers of Liao civilization or Yangtze civilization. As the Liao civilization and the Yangtze civilization declined several tribes crossed westward and northerly, to the Korean Peninsula and the Japanese archipelago. However, Mitsuru Sakitani said that Currently, very little o1b2 are detected in the Yangtze River region, there are many problems in the theory that originate from the Yangtze River area.[28][29][30] Another study calls the haplogroup O1b1 as the major Austroasiatic paternal lineage and the haplogroup O1b2 (of Koreans and Japanese) as the "para-Austroasiatic" paternal lineage.[31]
Subclade distribution
editParagroup O-M176*
editY-DNA that belongs to O-M176(xK10, F3356) has been found in an individual from Hiroshima,[4] an individual from Fukushima,[4] an individual from Beijing,[4] and 1% (7/706) of a sample of males collected in Seoul and Daejeon.[32]
O-M176(x47z) has been found in approximately 9.2% of Japanese males (ranging from 3.5% in the JPT sample from Tokyo[33] to 13.1% in a sample from Shizuoka[34]) and in approximately 8.3% of Ryukyuan males (ranging from 5.3% in a sample from Miyako[8] to 11.1% in a sample from Okinawa[34]).[6]
O-K10
editThe majority of extant members of O-M176 belong to the subclade O-K10 (aka O-F3356 aka O-F1204). O-K10 (TMRCA 8,070 ybp according to TheYtree,[35] 7,900 [95% CI 5,624 <-> 9,449] ybp according to Karmin et al. 2022,[1] 7,457 (99% CI 9,434 - 5,789) years before present according to FamilyTreeDNA,[36] 7,000 [95% CI 8,000 <-> 6,000] ybp according to YFull,[4] or 6,970 years according to 23mofang[2]) subsumes the prolific subclades O-47z, which occurs with especially high frequency in Japan, and O-L682, which occurs with especially high frequency in Korea, in addition to the relatively rare subclades O-CTS10687, which has been found in Japan, Korea, and China, and O-K3, which has been found among Han Chinese mostly in South Central China. O-L682 and O-K3 are linked by 18 SNPs that define the O-K4 clade, and thus their members are more closely related to one another by paternal lineage than any of them is related to any member of O-47z or O-CTS10687.
O-F3356(x47z, L682) has been found in 2% (14/706) of a sample of Koreans collected in Seoul and Daejeon, South Korea.[32] However, the status of these individuals' Y-DNA in regard to K4, K3, CTS10687, and phylogenetically equivalent SNPs has not been published.
O-CTS10687 has been found in 1.8% (1/56) of the JPT sample of Japanese from Tokyo, Japan.[37][4]
O-47z
editHaplogroup O-47z | |
---|---|
Possible time of origin | 7,870 [95% CI 5,720–12,630] years ago (Hammer et al. 2006) 7,613 (95% CI 5,309 <-> 9,130) ybp[1] 7,000 [95% CI 6,100 <-> 7,900] ybp[3] |
Coalescence age | 5,780 ybp[2] 5,600 (95% CI 6,500 <-> 4,700) ybp[4] |
Possible place of origin | Japanese Archipelago (Hammer et al. 2006) or Korean Peninsula (Jin et al. 2003) |
Ancestor | O-M176 |
Defining mutations | 47z |
Highest frequencies | Japanese, Ryukyuans, Koreans |
O-47z or O-CTS11986 is a subclade of O-K10. It is found with high frequency among the Japanese and Ryukyuan populations of Japan, and with lower frequency among Koreans.
Haplogroup O-47z has been detected in approximately 22% of males who speak a Japonic language, while it has not been found at all among Ainu males whose Y-DNA has been tested in two genetic studies (Tajima et al. 2004, n=16; Hammer et al. 2006, n=4). Based on the STR haplotype diversity within Haplogroup O-47z, it has been estimated in a study published in 2006 that this haplogroup has expanded from a single founder who has lived approximately 3,810 (95% CI 1,640 <–> 7,960) years before present in a model according to which continuous, pure exponential population growth is assumed.[11] In a paper published in 2016, the time to most recent common ancestor of a set of fifteen members of the O-47z clade, all from the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project, was estimated to be 4,500 years using a relatively slow mutation rate (μ = 0.76 x 10−9 per bp per year as according to Qiaomei Fu et al. 2014) or 3,900 years using a relatively fast mutation rate (μ = 0.888 x 10−9 per bp per year as according to A. Helgason et al. 2015).[33] Haplogroup O-47z also has been found among samples of modern Koreans, though with low frequency in comparison to both the frequency of O-47z in samples of Japanese and the frequency of O-M176(x47z) in samples of Koreans.[5]
Soon-Hee Kim et al. (2011) found haplogroup O-47z (DXYS5Y-Y2) in 8.89% (45/506) of a pool of samples from South Korea. O-47z was found in greatest proportion in the study's sample from the Gyeongsang region (10/84 = 11.9%), which is located in the southeast corner of the Korean Peninsula, and in least proportion in the study's sample from the Seoul-Gyeonggi region (8/110 = 7.3%), which is located on the west coast of the middle of the Korean Peninsula.[38] Haplogroup O-47z also has been observed in a sample of Koreans in China (2/25 = 8.0%).[39]
O-K4
editO-K4 is a subclade of O-K10. It includes at least two subclades, O-L682 and O-K3, which have been estimated to share a most recent common ancestor approximately 6,327 (95% CI 4,575 <-> 7,762) years before present.[1]
O-K3
editHaplogroup O-F940 | |
---|---|
Possible time of origin | 6,327 (95% CI 4,575 <-> 7,762) years before present[1] 6,000 years before present[2] 6,000 (95% CI 7,100 <-> 4,900) ybp[4] |
Coalescence age | 2,650 years before present[2] |
Possible place of origin | East Asia (origin) China (MRCA) |
Ancestor | O-F2868 |
Defining mutations | CTS12145, F1912, F2206, F2703, F940, K3 |
Highest frequencies | Chinese[4][1] 0.12%[2] |
The O-K3 (or O-F940) lineage is a subclade of O-K4 that has been observed to date in three individuals from Hunan,[4] one individual from Jiangxi,[4] and one individual from Henan.[19] The TMRCA of the three individuals from Hunan plus the one individual from Jiangxi has been estimated to be 1,300 (95% CI 800 <-> 2,100) ybp.[4]
O-L682
editHaplogroup O-L682 | |
---|---|
Possible time of origin | 6,327 [95% CI 4,575 <-> 7,762] ybp[1] 5,990 ybp[2] |
Coalescence age | 4,080 ybp[2] 4,200 (95% CI 4,900 <-> 3,500) ybp[4] |
Possible place of origin | Korean Peninsula or Manchuria |
Ancestor | O-M176, O-F3356 |
Defining mutations | L682 |
Highest frequencies | Koreans, Japanese, Ryukyuans, Hezhen, Manchus |
The O-L682 subclade of O-K4 is believed to be related to Native Korean population. One study has found O-L682 Y-DNA in 19% (134/706) of Koreans sampled in Seoul and Daejeon.[32] O-L682 also has been found in Japanese in Tokyo, Okayama, Kōchi, and the US and in Chinese (especially in Jilin, Heilongjiang, and Liaoning, with a greater than average presence also in Beijing, Hebei, Inner Mongolia, Gansu, Shaanxi, Shandong, Tianjin, and Anhui,[2] and with some presence in other areas, such as Shanxi,[4] and among some ethnic minorities, such as Nanai people[4]). Its descendants appear to have begun rapidly increasing in number at approximately the same time as those of its distant cousin O-47z, perhaps 4,000 years ago.[4]
Phylogenetics
editPhylogenetic history
editPrior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
YCC 2002/2008 (Shorthand) |
(α) | (β) | (γ) | (δ) | (ε) | (ζ) | (η) | YCC 2002 (Longhand) |
YCC 2005 (Longhand) |
YCC 2008 (Longhand) |
YCC 2010r (Longhand) |
ISOGG 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
O-M175 | 26 | VII | 1U | 28 | Eu16 | H9 | I | O* | O | O | O | O | O | O | O | O | O | O |
O-M119 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1* | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a |
O-M101 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1a | O1a1 | O1a1a | O1a1a | O1a1 | O1a1 | O1a1a | O1a1a | O1a1a | O1a1a | O1a1a |
O-M50 | 26 | VII | 1U | 32 | Eu16 | H10 | H | O1b | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 |
O-P31 | 26 | VII | 1U | 33 | Eu16 | H5 | I | O2* | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 |
O-M95 | 26 | VII | 1U | 34 | Eu16 | H11 | G | O2a* | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a1 | O2a1 |
O-M88 | 26 | VII | 1U | 34 | Eu16 | H12 | G | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1a | O2a1a |
O-SRY465 | 20 | VII | 1U | 35 | Eu16 | H5 | I | O2b* | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b |
O-47z | 5 | VII | 1U | 26 | Eu16 | H5 | I | O2b1 | O2b1a | O2b1 | O2b1 | O2b1a | O2b1a | O2b1 | O2b1 | O2b1 | O2b1 | O2b1 |
O-M122 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3* | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 |
O-M121 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3a | O3a | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1a | O3a1a |
O-M164 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3b | O3b | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a1b | O3a1b |
O-M159 | 13 | VII | 1U | 31 | Eu16 | H6 | L | O3c | O3c | O3a3a | O3a3a | O3a3 | O3a3 | O3a3a | O3a3a | O3a3a | O3a3a | O3a3a |
O-M7 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d* | O3c | O3a3b | O3a3b | O3a4 | O3a4 | O3a3b | O3a3b | O3a3b | O3a2b | O3a2b |
O-M113 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d1 | O3c1 | O3a3b1 | O3a3b1 | - | O3a4a | O3a3b1 | O3a3b1 | O3a3b1 | O3a2b1 | O3a2b1 |
O-M134 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e* | O3d | O3a3c | O3a3c | O3a5 | O3a5 | O3a3c | O3a3c | O3a3c | O3a2c1 | O3a2c1 |
O-M117 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1* | O3d1 | O3a3c1 | O3a3c1 | O3a5a | O3a5a | O3a3c1 | O3a3c1 | O3a3c1 | O3a2c1a | O3a2c1a |
O-M162 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1a | O3d1a | O3a3c1a | O3a3c1a | O3a5a1 | O3a5a1 | O3a3c1a | O3a3c1a | O3a3c1a | O3a2c1a1 | O3a2c1a1 |
Original research publications
editThe following research teams per their publications were represented in the creation of the YCC Tree.
Phylogenetic trees
editThis phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree (Karafet et al. 2008) and subsequent published research.
- O1b2 (IMS-JST022454, L272.2, M176/Page63/SRY465, M302, P49, F1942/Page92)
- O1b2a (F1942/Page92)
- O1b2a1 (CTS9259)
- O1b2a1a (F3356)
- O1b2a1a1 (47z, CTS713, CTS11986)
- O1b2a1a2 (F2868, F3110, K4)
- O1b2a1a2a (L682)
- O1b2a1a2b (F940, F1912, F3390)
- O1b2a1a3 (CTS10687, F1813, F1800)
- O1b2a1b (CTS562)
- O1b2a1a (F3356)
- O1b2a2 (Page90)
- O1b2a1 (CTS9259)
- O1b2a (F1942/Page92)
Table of frequencies of O-M176
editPopulation | Frequency | Sample Size | SNPs | Source |
---|---|---|---|---|
Korean (Gangwon) | 0.397 | 63 | M176(x47z)=20 47z=5 |
Kim et al. 2011 |
Korean (National Biobank of Korea) |
0.377 | 300 | M176(x47z)=88 47z=25 |
Park 2013 |
Korean (South Korea) | 0.373 | 75 | M176/P49(x47z)=25 47z=3 |
Hammer et al. 2006 |
Japanese (Fukuoka) | 0.353 | 102 | 47z=27 M176(x47z)=9 |
Sato 2014 |
Japanese (Shizuoka) | 0.344 | 61 | 47z=13 M176/P49(x47z)=8 |
Hammer et al. 2006 |
Japanese (Kawasaki) | 0.343 | 321 | 47z=78 M176(x47z)=32 |
Sato 2014 |
Japanese (Nagasaki) | 0.340 | 300 | 47z=70 M176(x47z)=32 |
Sato 2014 |
Korean (Daejeon) | 0.338 | 133 | M176(x47z)=30 47z=15 |
Park 2012 |
Japanese (Tokushima) | 0.335 | 388 | 47z=90 M176(x47z)=40 |
Sato 2014 |
Japanese | 0.335 | 263 | 47z=66 M176/JST022454(x47z)=22 |
Nonaka, Minaguchi & Takezaki 2007 |
Japanese (male students in Kanazawa) | 0.326 | 298 | 47z=63 M176(x47z)=34 |
Sato 2014 |
Korean (Jeju) | 0.322 | 87 | M176(x47z)=20 47z=8 |
Kim et al. 2011 |
Japanese | 0.322 | 432 | M176=139 | Harayama 2014 |
Japanese (Tokyo) | 0.321 | 56 | 47z=15 CTS10687=1 L682(xCTS723)=1 CTS723=1 |
Poznik 2016 |
Japanese (Kyushu) | 0.321 | 53 | 47z=15 M176/P49(x47z)=2 |
Hammer et al. 2006 |
Japanese (male students in Sapporo) | 0.318 | 302 | 47z=70 M176(x47z)=26 |
Sato 2014 |
Korean (Seoul) | 0.316 | 573 | M176(x47z)=125 47z=56 |
Park 2012 |
Korean (Jeolla) | 0.311 | 90 | M176(x47z)=21 47z=7 |
Kim et al. 2011 |
Japanese (Aomori) | 0.308 | 26 | 47z=7 M176/P49(x47z)=1 |
Hammer et al. 2006 |
Korean (Chungcheong) | 0.306 | 72 | M176(x47z)=15 47z=7 |
Kim et al. 2011 |
Japanese (Hachinohe Kita High School & Sanbongi High School) | 0.304 | 79 | 47z=18 M176(x47z)=6 |
Totsuka 2016 |
Japanese (Tokushima) | 0.300 | 70 | 47z=17 M176/P49(x47z)=4 |
Hammer et al. 2006 |
Korean (Gyeongsang) | 0.298 | 84 | M176(x47z)=15 47z=10 |
Kim et al. 2011 |
Japanese | 0.293 | 157 | 47z=38 M176(x47z)=8 |
Kim et al. 2011 |
Okinawa (Miyako High School) | 0.289 | 38 | 47z=9 M176(x47z)=2 |
Totsuka 2016 |
Japanese (Osaka) | 0.282 | 241 | 47z=43 M176(x47z)=25 |
Sato 2014 |
Korean (Seoul/Gyeonggi) | 0.282 | 110 | M176(x47z)=23 47z=8 |
Kim et al. 2011 |
Japanese (adult males in Kanazawa) | 0.280 | 232 | 47z=43 M176(x47z)=22 |
Sato 2014 |
Korean (PRC) | 0.280 | 25 | M176(x47z)=5 47z=2 |
Xue et al. 2006 |
Korean (Korea) | 0.279 | 43 | M176(x47z)=6 47z=6 |
Xue et al. 2006 |
Japanese (adult males in Sapporo) | 0.277 | 206 | 47z=41 M176(x47z)=16 |
Sato 2014 |
Japanese (Kagawa) | 0.277 | 47 | 47z=11 M176(x47z)=2 |
Xue et al. 2006 |
Japanese (Saga) | 0.271 | 129 | 47z=24 M176(x47z)=11 |
Totsuka 2016 |
Manchurians | 0.271 | 48 | 47z=9 M176(x47z)=4 |
Jin, Kim & Kim 2010 |
Korean (Seoul & Daejeon) | 0.269 | 216 | M176(x47z)=37 47z=21 |
Kim et al. 2007 |
Okinawa (Yaeyama High School & Yaeyama Commercial and Technical High School) | 0.265 | 49 | 47z=9 M176(x47z)=4 |
Totsuka 2016 |
Japanese | 0.262 | 107 | 47z=21 M176(x47z)=7 |
Jin, Kim & Kim 2010 |
Okinawa | 0.222 | 45 | 47z=5 M176/P49(x47z)=5 |
Hammer et al. 2006 |
Korean | 0.201 | 154 | M176(x47z)=22 47z=9 |
Jin, Kim & Kim 2010 |
Okinawa (Kaihō High School) | 0.194 | 36 | 47z=4 M176(x47z)=3 |
Totsuka 2016 |
Udeges | 0.095 | 21 | M176(x47z)=2 | Jin, Kim & Kim 2010 |
Han (Beijing) | 0.020 | 51 | M176(x47z)=1 | Kim et al. 2011 |
Manchu | 0.057 | 35 | M176(x47z)=2 | Xue et al. 2006 |
Uriankhai (Mongolia) | 0.050 | 60 | M176=3 | Katoh et al. 2005 |
Mongol (NE Mongolia) | 0.050 | 20 | M176=1 | Di Cristofaro et al. 2013 harvnb error: multiple targets (2×): CITEREFDi_CristofaroPennarunMazièresMyres2013 (help) |
Hezhe (PRC) | 0.044 | 45 | M176(x47z)=2 | Xue et al. 2006 |
Manchu | 0.038 | 52 | M176/P49(x47z)=2 | Hammer et al. 2006 |
Zakhchin (Mongolia) | 0.033 | 60 | M176=2 | Katoh et al. 2005 |
Manchurian | 0.033 | 30 | M176(x47z)=1 | Kim et al. 2011 |
Hakka (Taiwan) | 0.029 | 34 | M176=1 | Trejaut et al. 2014 |
Buryat | 0.028 | 36 | M176(x47z)=1 | Kim et al. 2011 |
Nanai (Samar from Khabarovsk) |
≤0.027 | 37 | O-P31=1 | Bogunov et al. 2015 |
Daur | 0.026 | 39 | M176(x47z)=1 | Xue et al. 2006 |
Evenk (PRC) | 0.024 | 41 | M176/P49(x47z)=1 | Hammer et al. 2006 |
Xibe | 0.024 | 41 | M176(x47z)=1 | Xue et al. 2006 |
Buryat | 0.020 | 50 | M176(x47z)=1 | Jin, Kim & Kim 2010 |
Mongols (Mongolia) | 0.006 | 160 | M176=1 | Di Cristofaro et al. 2013 harvnb error: multiple targets (2×): CITEREFDi_CristofaroPennarunMazièresMyres2013 (help) |
Han (Taiwan) | 0.004 | 258 | M176=1 | Trejaut et al. 2014 |
Zhuang | 0.000 | 20 | M176/P49=0 | Hammer et al. 2006 |
Oroqen | 0.000 | 22 | M176/P49=0 | Hammer et al. 2006 |
Hanoi, Vietnam | 0.000 | 24 | M176=0 | Trejaut et al. 2014 |
Kalimantan | 0.000 | 25 | M176=0 | Trejaut et al. 2014 |
Evenk (PRC) | 0.000 | 26 | M176=0 | Xue et al. 2006 |
Sumatra | 0.000 | 26 | M176=0 | Trejaut et al. 2014 |
Akha (Thailand) | 0.000 | 27 | M176=0 | Trejaut et al. 2014 |
Alor | 0.000 | 28 | M176=0 | Karafet et al. 2010 |
Han (Lanzhou) | 0.000 | 30 | M176=0 | Xue et al. 2006 |
Even | 0.000 | 31 | M176/P49=0 | Hammer et al. 2006 |
Oroqen | 0.000 | 31 | M176=0 | Xue et al. 2006 |
Uyghur (Ürümqi) | 0.000 | 31 | M176=0 | Xue et al. 2006 |
Han (Yili) | 0.000 | 32 | M176=0 | Xue et al. 2006 |
Malay | 0.000 | 32 | M176/P49=0 | Hammer et al. 2006 |
Australian aborigines | 0.000 | 33 | M176/P49=0 | Hammer et al. 2006 |
Qiang | 0.000 | 33 | M176=0 | Xue et al. 2006 |
Han (Chengdu) | 0.000 | 34 | M176=0 | Xue et al. 2006 |
Hani (PRC) | 0.000 | 34 | M176=0 | Xue et al. 2006 |
Li | 0.000 | 34 | M176=0 | Xue et al. 2006 |
She | 0.000 | 34 | M176=0 | Xue et al. 2006 |
Buyi | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Han (Harbin) | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Han (Meixian) | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Hui (PRC) | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Tibetan | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Yao (Bama) | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Yao (Liannan) | 0.000 | 35 | M176=0 | Xue et al. 2006 |
Batak Toba (Sumatra) | 0.000 | 38 | M176=0 | Karafet et al. 2010 |
Uyghur (Yili) | 0.000 | 39 | M176=0 | Xue et al. 2006 |
East Indonesia | 0.000 | 40 | M176=0 | Trejaut et al. 2014 |
Han (Guangdong) | 0.000 | 40 | M176/P49=0 | Hammer et al. 2006 |
Yi (Butuo, Sichuan) | 0.000 | 43 | M176/P49=0 | Hammer et al. 2006 |
Northern Han | 0.000 | 44 | M176/P49=0 | Hammer et al. 2006 |
Khalkh | 0.000 | 45 | M176=0 | Kim et al. 2011 |
Mongol (Inner Mongolia) | 0.000 | 45 | M176=0 | Xue et al. 2006 |
Papua New Guinea | 0.000 | 46 | M176/P49=0 | Hammer et al. 2006 |
Khalkh | 0.000 | 48 | M176=0 | Jin, Kim & Kim 2010 |
Philippines | 0.000 | 48 | M176/P49=0 | Hammer et al. 2006 |
Taiwanese aborigines | 0.000 | 48 | M176/P49=0 | Hammer et al. 2006 |
Tujia | 0.000 | 49 | M176/P49=0 | Hammer et al. 2006 |
She | 0.000 | 51 | M176/P49=0 | Hammer et al. 2006 |
Melanesia | 0.000 | 53 | M176/P49=0 | Hammer et al. 2006 |
Mandar (Sulawesi) | 0.000 | 54 | M176=0 | Karafet et al. 2010 |
Han (Fujian) | 0.000 | 55 | M176=0 | Trejaut et al. 2014 |
Indonesia (East) | 0.000 | 55 | M176/P49=0 | Hammer et al. 2006 |
Miao | 0.000 | 58 | M176/P49=0 | Hammer et al. 2006 |
Han (Yunnan) | 0.000 | 60 | M176=0 | Kim et al. 2011 |
Minnan (Taiwan) | 0.000 | 60 | M176=0 | Trejaut et al. 2014 |
Nias | 0.000 | 60 | M176=0 | Karafet et al. 2010 |
Polynesia | 0.000 | 60 | M176/P49=0 | Hammer et al. 2006 |
Yao | 0.000 | 60 | M176/P49=0 | Hammer et al. 2006 |
Java | 0.000 | 61 | M176=0 | Karafet et al. 2010 |
Filipino | 0.000 | 64 | M176=0 | Kim et al. 2011 |
Mongol (Outer Mongolia) | 0.000 | 65 | M176=0 | Xue et al. 2006 |
Uyghur | 0.000 | 67 | M176/P49=0 | Hammer et al. 2006 |
Mentawai | 0.000 | 74 | M176=0 | Karafet et al. 2010 |
Thailand | 0.000 | 75 | M176=0 | Trejaut et al. 2014 |
Buryat | 0.000 | 81 | M176/P49=0 | Hammer et al. 2006 |
Han (Taiwan) | 0.000 | 84 | M176/P49=0 | Hammer et al. 2006 |
Borneo | 0.000 | 86 | M176=0 | Karafet et al. 2010 |
Sri Lanka | 0.000 | 91 | M176/P49=0 | Hammer et al. 2006 |
Lembata | 0.000 | 92 | M176=0 | Karafet et al. 2010 |
Evenk (Russia) | 0.000 | 95 | M176/P49=0 | Hammer et al. 2006 |
Altai | 0.000 | 98 | M176/P49=0 | Hammer et al. 2006 |
Tibet | 0.000 | 105 | M176/P49=0 | Hammer et al. 2006 |
Java | 0.000 | 141 | M176=0 | Trejaut et al. 2014 |
Philippines | 0.000 | 146 | M176=0 | Trejaut et al. 2014 |
Mongolia | 0.000 | 149 | M176/P49=0 | Hammer et al. 2006 |
Sumba | 0.000 | 350 | M176=0 | Karafet et al. 2010 |
Taiwan mountain tribes | 0.000 | 355 | M176=0 | Trejaut et al. 2014 |
Taiwan plains tribes | 0.000 | 370 | M176=0 | Trejaut et al. 2014 |
Flores | 0.000 | 394 | M176=0 | Karafet et al. 2010 |
India | 0.000 | 405 | M176/P49=0 | Hammer et al. 2006 |
Bali | 0.000 | 641 | M176=0 | Karafet et al. 2010 |
See also
editGenetics
editY-DNA O subclades
editY-DNA backbone tree
editReferences
editFootnotes
edit- ^ 256/800=32.0% O-M176 in a pool of all Japanese samples of (Xue et al. 2006), (Katoh et al. 2005), (Jin, Kim & Kim 2010), (Nonaka, Minaguchi & Takezaki 2007), (Poznik et al. 2016), and all non-Ainu and non-Okinawan Japanese samples of (Hammer et al. 2006).
- ^ 202/677=29.8% O-M176 in a pool of all ethnic South Korean samples of (Hammer et al. 2006), (Xue et al. 2006), (Katoh et al. 2005), (Kim et al. 2007), and (Park 2013)
- ^ 61/255=23.92% O-M176 in a pool of all Ryukyuan data from (Hammer et al. 2006), (Nonaka, Minaguchi & Takezaki 2007), and Totsuka et al. 2016
- ^ 30/123=24.3% O-M176 in a pool of all ethnic North Korea samples of (Jeong 2018)
- ^ 733/3271 = 22.41% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Hammer et al. 2006), (Xue et al. 2006), (Nonaka, Minaguchi & Takezaki 2007), Kim et al. 2011, Sato et al. 2014, and Totsuka et al. 2016
- ^ 44/255 = 17.3% O-47z in a pool of all Okinawan samples of (Hammer et al. 2006), (Nonaka, Minaguchi & Takezaki 2007), and Totsuka et al. 2016
- ^ 299/3271 = 9.14% O-P49(x47z) in a pool of all non-Ainu and non-Okinawan Japanese samples of (Hammer et al. 2006), (Xue et al. 2006), (Nonaka, Minaguchi & Takezaki 2007), Kim et al. 2011, Sato et al. 2014, and Totsuka et al. 2016
- ^ 17/255 = 6.7% O-P49(x47z) in a pool of all Okinawan samples of (Hammer et al. 2006), (Nonaka, Minaguchi & Takezaki 2007), and Totsuka et al. 2016
Citations
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edit- Jin HJ, Tyler-Smith C, Kim W (2009). Batzer MA (ed.). "The peopling of Korea revealed by analyses of mitochondrial DNA and Y-chromosomal markers". PLOS ONE. 4 (1): e4210. Bibcode:2009PLoSO...4.4210J. doi:10.1371/journal.pone.0004210. PMC 2615218. PMID 19148289.
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- Balaresque P, Poulet N, Cussat-Blanc S, Gerard P, Quintana-Murci L, Heyer E, Jobling MA (October 2015). "Y-chromosome descent clusters and male differential reproductive success: young lineage expansions dominate Asian pastoral nomadic populations". European Journal of Human Genetics. 23 (10): 1413–1422. doi:10.1038/ejhg.2014.285. PMC 4430317. PMID 25585703.