A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698639



Internal ID15088605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122924980..122928522hg38UCSC Ensembl
Innerchr11:122795688..122799230hg19UCSC Ensembl
Innerchr11:122300898..122304440hg18UCSC Ensembl
Innerchr11:122300898..122304440hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg383543
hg193543
hg183543
hg173543
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522969
Supporting Variants
Samples
Known GenesC11orf63
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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