A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774760



Internal ID16068716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55203117hg38UCSC Ensembl
Innerchr11:54695707..54970593hg19UCSC Ensembl
Innerchr11:54452283..54727169hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38274886
hg19274887
hg18274887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554613
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv774760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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