A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518797



Internal ID15446090
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696252
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518797
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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