Draft:Haplogroup O-M176

Haplogroup O-M176
Possible time of origin31,108 (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 age25,660 years before present[2]

25,800 [95% CI 23,400 <-> 28,400] years before present (YFull[3][4])
Possible place of originthe Korean Peninsula or a nearby part of northeastern Asia[5]
AncestorO-P31
Defining mutationsM176/SRY465, P49, 022454[citation needed]
Highest frequenciesJapanese, 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

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Haplogroup 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

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Paragroup O-M176*

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Y-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

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The 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

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Haplogroup O-47z
Possible time of origin7,870 [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 age5,780 ybp[2]

5,600 (95% CI 6,500 <-> 4,700) ybp[4]
Possible place of originJapanese Archipelago (Hammer et al. 2006) or Korean Peninsula (Jin et al. 2003)
AncestorO-M176
Defining mutations47z
Highest frequenciesJapanese, 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

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O-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
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Haplogroup O-F940
Possible time of origin6,327 (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 age2,650 years before present[2]
Possible place of originEast Asia (origin)
China (MRCA)
AncestorO-F2868
Defining mutationsCTS12145, F1912, F2206, F2703, F940, K3
Highest frequenciesChinese[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
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Haplogroup O-L682
Possible time of origin6,327 [95% CI 4,575 <-> 7,762] ybp[1]

5,990 ybp[2]
Coalescence age4,080 ybp[2]

4,200 (95% CI 4,900 <-> 3,500) ybp[4]
Possible place of originKorean Peninsula or Manchuria
AncestorO-M176, O-F3356
Defining mutationsL682
Highest frequenciesKoreans, 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

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Phylogenetic history

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Prior 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

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The following research teams per their publications were represented in the creation of the YCC Tree.

Phylogenetic trees

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This 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)
      • O1b2a2 (Page90)

Table of frequencies of O-M176

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Population 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

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Genetics

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Y-DNA O subclades

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Y-DNA backbone tree

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References

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Footnotes

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  1. ^ 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).
  2. ^ 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)
  3. ^ 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
  4. ^ 30/123=24.3% O-M176 in a pool of all ethnic North Korea samples of (Jeong 2018)
  5. ^ 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
  6. ^ 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
  7. ^ 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
  8. ^ 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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  1. ^ a b c d e f g h Monika Karmin, Rodrigo Flores, Lauri Saag, et al. (2022), "Episodes of Diversification and Isolation in Island Southeast Asian and Near Oceanian Male Lineages." Mol. Biol. Evol. 39(3): msac045 doi:10.1093/molbev/msac045
  2. ^ a b c d e f g h i j k l m n o p q Phylogenetic tree of haplogroup O-M268 at 23mofang
  3. ^ a b c d YFull Haplogroup YTree v6.01 at 04 January 2018
  4. ^ a b c d e f g h i j k l m n o p YFull Haplogroup YTree v5.04 at 16 May 2017
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  41. ^ HGDP 2009.

Sources

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Further reading

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