Human (GRCh37.p13)
Variation class
Allele type(s)
Source

DGVa - Database of Genomic Variants Archive

Study

nstd37 - International Standards for Cytogenetic Array Consortium

Alias

13___99434951_99436576___NCBI36_copy_number_variation

Location

Chromosome 13:100636950-100638575 (forward strand) | View in location tab

Genomic size

1,626 bp

About this structural variant

This structural variant overlaps 5 transcripts, is associated with 1 phenotype and is supported by 1 piece of evidence.