A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764585



Internal ID16058541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3247045..3309838hg38UCSC Ensembl
Innerchr11:3268275..3331068hg19UCSC Ensembl
Innerchr11:3224851..3287644hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3862794
hg1962794
hg1862794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553132
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)nssv764585
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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