DNA Marker Index information for Chromosome: Y Marker: CTS10513.1
Names and Aliases for this DNA Marker: CTS10513.1, CTS10513, M5282, PF1789, V4197.1, V4197, rs367824482.
Chromosome Position in hg38 Human Genome assembly1: 17391820.
Chromosome Position in hg19 assembly2: 19503700 .
Ancestral marker allele value: T.
Derived, alternative, or mutated marker allele value: C.


DNA Marker Index data for Marker: CTS10513.1 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
CTS10513.1 CTS10513 M5282 PF1789 V4197.1 V4197 rs367824482
 Found in haplogroup E1b with M215 on 23mofang, YFull, and FTDNA trees. See also CTS10513.2 in haplogroup O2a. See also CTS10513.3 in haplogroup J1a. See also CTS10513.4 in haplogroup R1a.
DNA lineage CTS10513.1 is estimated to have originated in about the year 46,000 bce based on its position in the phylogenetic tree.
Coincident with M215. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 18013094 		Chris Tyler-Smith 2011
T
C
Y
 17391820
19503700

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