A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665009



Internal ID15401661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110089850..110109174hg38UCSC Ensembl
Innerchr13:110742197..110761521hg19UCSC Ensembl
Innerchr13:109540198..109559522hg18UCSC Ensembl
Innerchr13:109540198..109559522hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3819325
hg1919325
hg1819325
hg1719325
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515849
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665009
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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