A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697546



Internal ID15087512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73288176..73350811hg38UCSC Ensembl
Innerchr11:72999221..73061856hg19UCSC Ensembl
Innerchr11:72676869..72739504hg18UCSC Ensembl
Innerchr11:72676869..72739504hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3862636
hg1962636
hg1862636
hg1762636
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520665
Supporting Variants
Samples
Known GenesARHGEF17, P2RY6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697546
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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