A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553132



Internal ID16340541
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 StatusM
Merged Variantsdgv1579n54
Supporting Variantsnssv764586, nssv764585, nssv764583, nssv764584, nssv764582
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553132
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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