A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697996



Internal ID15434648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79634818..79637802hg38UCSC Ensembl
Innerchr11:79345862..79348846hg19UCSC Ensembl
Innerchr11:79023510..79026494hg18UCSC Ensembl
Innerchr11:79023510..79026494hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382985
hg192985
hg182985
hg172985
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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