Variation class
CNV(SO:0001019)
Allele type(s)
gain(SO:0001742)
loss(SO:0001743)
Source
DGVa - Database of Genomic Variants Archive
Study
nstd45 - International Standards for Cytogenomic Arrays Consortium (curated dataset) PMID:21844811 PMID:20466091
Alias
ISCA_3_VAR_46
Clinical significance 
Location
Chromosome 2:110122329-110205017 (forward strand) | View in location tab
Genomic size
82,689 bp
About this structural variant
This structural variant overlaps 1 transcript, is associated with 1 phenotype and is supported by 2 pieces of evidence.