Variation class
sequence alteration(SO:0001059)
Allele type(s)
CNV(SO:0001019)
Source
DGVa - Database of Genomic Variants Archive
Study
estd20 - Conrad 2010 "Origins and functional impact of copy number variation in the human genome." PMID:19812545
Alias
CNVR4245
Location
Chromosome 9:35372372-35375252 (forward strand) | View in location tab
About this structural variant
This structural variant overlaps 8 transcripts and is supported by 1 piece of evidence.
