Variation class
CNV(SO:0001019)
Allele type(s)
deletion(SO:0000159)
Source
DGVa - Database of Genomic Variants Archive
Study
estd199 - 1000 Genomes Project Consortium - Phase 1. PMID:23128226
Location
Chromosome 21:46906165-46906372 (forward strand) | View in location tab
Genomic size
208 bp
About this structural variant
This structural variant overlaps 3 transcripts and is supported by 91 pieces of evidence.
