Human (GRCh37.p13)
Variation class

indel(SO:1000032)

Allele type(s)

indel(SO:1000032)

Source

DGVa - Database of Genomic Variants Archive

Study

estd214 - 1000 Genomes Project Consortium - Phase 3

Alias

PHASE3_V1_SV_1259_A1

Present in

1000 Genomes 3 - All (1000 Genomes 3 - AFR, 1000 Genomes 3 - AMR)

Location

Chromosome 10:93644869 (forward strand) | View in location tab

About this structural variant

This structural variant is supported by 18 pieces of evidence.