A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696252



Internal ID15432904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123945507..123976157hg38UCSC Ensembl
Innerchr11:123816214..123846864hg19UCSC Ensembl
Innerchr11:123321424..123352074hg18UCSC Ensembl
Innerchr11:123321424..123352074hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3830651
hg1930651
hg1830651
hg1730651
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518797
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696252
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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