A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694784



Internal ID15431436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80118676..80127713hg38UCSC Ensembl
Innerchr13:80692811..80701848hg19UCSC Ensembl
Innerchr13:79590812..79599849hg18UCSC Ensembl
Innerchr13:79590812..79599849hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg389038
hg199038
hg189038
hg179038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522015
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694784
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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