A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117121



Internal ID21300387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100686355..100688942hg38UCSC Ensembl
Innerchr11:100557086..100559673hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382588
hg192588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093200
Samplessample348
Known GenesARHGAP42
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117121
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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