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In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by specific mutations in the non-recombining portions of DNA on the male-specific Y chromosome (Y-DNA). Individuals within a haplogroup share similar numbers of short tandem repeats (STRs) and single-nucleotide polymorphisms (SNPs). [ 2 ]
Y-DNA haplogroups by ethnic group; Y-DNA haplogroups in populations of Europe; Y-DNA haplogroups in populations of the Caucasus; Y-DNA haplogroups in populations of the Near East; Y-DNA haplogroups in populations of North Africa; Y-DNA haplogroups in populations of Sub-Saharan Africa; Y-DNA haplogroups in populations of South Asia
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In human population genetics, Y-Chromosome haplogroups define the major lineages of direct paternal (male) lines back to a shared common ancestor in Africa. Men in the same haplogroup share a set of differences, or markers, on their Y-Chromosome, which distinguish them from men in other haplogroups.
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A haplotype is a group of alleles in an organism that are inherited together from a single parent, [1] [2] and a haplogroup (haploid from the Greek: ἁπλοῦς, haploûs, "onefold, simple" and English: group) is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. [3]
Y-DNA haplogroups by group. Y-DNA haplogroups in populations of South Asia; Y-DNA haplogroups in populations of Central and North Asia; Y-DNA haplogroups in populations of Oceania; Y-DNA haplogroups in populations of the Near East; Y-DNA haplogroups in populations of North Africa; Y-DNA haplogroups in populations of Europe; Y-DNA haplogroups in ...