Human (GRCh37.p13)
Variation class

complex alteration(SO:0001784)

Allele type(s)

complex alteration(SO:0001784)

Source

DGVa - Database of Genomic Variants Archive

Study

estd176 - Banerjee 2011 "A computational framework discovers new copy number variants with functional importance." PMID:21479260 [remapped from build NCBI36]

Alias

IgH3.2139

Location

Chromosome 15:53682368-53683303 (forward strand) | View in location tab
Inner coordinates: 15:53682426-53683037

About this structural variant

This structural variant is supported by 1 piece of evidence.