A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694779



Internal ID15431431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111403113..111412665hg38UCSC Ensembl
Innerchr3:111121960..111131512hg19UCSC Ensembl
Innerchr3:112604650..112614202hg18UCSC Ensembl
Innerchr3:112604650..112614202hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg389553
hg199553
hg189553
hg179553
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522010
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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