A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552760



Internal ID16340169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:195956..198510hg38UCSC Ensembl
Innerchr11:195956..198510hg19UCSC Ensembl
Innerchr11:185956..188510hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382555
hg192555
hg182555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763038
Samples
Known GenesODF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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