A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111247



Internal ID21294513
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 StatusM
Merged Variants
Supporting Variantsnssv14090275
Samplessample404
Known GenesYAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111247
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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