Variation class
CNV(SO:0001019)
Allele type(s)
gain(SO:0001742)
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."
Alias
13___99434951_99436576___NCBI36_copy_number_variation
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.