A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698406



Internal ID15088372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44585782..44592121hg38UCSC Ensembl
Innerchr11:44607332..44613671hg19UCSC Ensembl
Innerchr11:44563908..44570247hg18UCSC Ensembl
Innerchr11:44563908..44570247hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386340
hg196340
hg186340
hg176340
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522766
Supporting Variants
Samples
Known GenesCD82
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698406
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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