A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110234



Internal ID21293500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102109864..102112248hg38UCSC Ensembl
Innerchr11:101980595..101982979hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382385
hg192385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091876
Samplessample224
Known GenesYAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110234
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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