A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671512



Internal ID15061478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113399438..113400106hg38UCSC Ensembl
Innerchr11:113270160..113270828hg19UCSC Ensembl
Innerchr11:112775370..112776038hg18UCSC Ensembl
Innerchr11:112775370..112776038hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38669
hg19669
hg18669
hg17669
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)nssv671512
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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