A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681276



Internal ID15417928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110089850..110107364hg38UCSC Ensembl
Innerchr13:110742197..110759711hg19UCSC Ensembl
Innerchr13:109540198..109557712hg18UCSC Ensembl
Innerchr13:109540198..109557712hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3817515
hg1917515
hg1817515
hg1717515
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)nssv681276
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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