Variation class
Allele type(s)
Source

DGVa - Database of Genomic Variants Archive

Study

nstd37 - Miller 2010 "Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies." PMID:20466091

Alias

ISCA_VAR_v5_860

Clinical significance

Location

Chromosome 13:99984696-99986321 (forward strand) | View in location tab

Genomic size

1,626 bp

About this structural variant

This structural variant overlaps 6 transcripts, is associated with 1 phenotype and is supported by 1 piece of evidence.

Structural variation displays