A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764568



Internal ID16058524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3247045..3296815hg38UCSC Ensembl
Innerchr11:3268275..3318045hg19UCSC Ensembl
Innerchr11:3224851..3274621hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3849771
hg1949771
hg1849771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553131
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)nssv764568
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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