Variation class
CNV(SO:0001019)
Allele type(s)
deletion(SO:0000159)
Source
DGVa - Database of Genomic Variants Archive
Study
estd180 - Pang 2010 "Towards a comprehensive structural variation map of an individual human genome." PMID:20482838 [remapped from build NCBI36]
Location
Chromosome 19:33306051-33306086 (forward strand) | View in location tab
Genomic size
36 bp
About this structural variant
This structural variant overlaps 1 transcript and is supported by 1 piece of evidence.
