A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525321



Internal ID15105928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44575267..44580406hg38UCSC Ensembl
Innerchr11:44596817..44601956hg19UCSC Ensembl
Innerchr11:44553393..44558532hg18UCSC Ensembl
Innerchr11:44553393..44558532hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385140
hg195140
hg185140
hg175140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701431
Samples
Known GenesCD82
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525321
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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