A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556141



Internal ID15996864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102117330..102337120hg38UCSC Ensembl
Innerchr11:101988061..102207851hg19UCSC Ensembl
Innerchr11:101493271..101713061hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38219791
hg19219791
hg18219791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv782007
Samples
Known GenesBIRC3, YAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556141
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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