A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657982



Internal ID15394634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134706322..134728149hg38UCSC Ensembl
Innerchr11:134576216..134598043hg19UCSC Ensembl
Innerchr11:134081426..134103253hg18UCSC Ensembl
Innerchr11:134081426..134103253hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3821828
hg1921828
hg1821828
hg1721828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657982
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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