A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689966



Internal ID15426618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76934907..76998751hg38UCSC Ensembl
Innerchr11:76645951..76709795hg19UCSC Ensembl
Innerchr11:76323599..76387443hg18UCSC Ensembl
Innerchr11:76323599..76387443hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3863845
hg1963845
hg1863845
hg1763845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519700
Supporting Variants
Samples
Known GenesACER3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689966
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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