A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090275



Internal ID21287652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102107729..102115326hg38UCSC Ensembl
Innerchr11:101978460..101986057hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg387598
hg197598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111247
Supporting Variants
Samplessample404
Known GenesYAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090275
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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