A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687146



Internal ID15077112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113396099..113399652hg38UCSC Ensembl
Innerchr11:113266821..113270374hg19UCSC Ensembl
Innerchr11:112772031..112775584hg18UCSC Ensembl
Innerchr11:112772031..112775584hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383554
hg193554
hg183554
hg173554
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515795
Supporting Variants
Samples
Known GenesANKK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687146
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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