A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111232



Internal ID21294498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33845835..33848833hg38UCSC Ensembl
Innerchr22:34241823..34244821hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382999
hg192999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104006
Samplessample417
Known GenesLARGE
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111232
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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