A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116797



Internal ID21300063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34342080..34518083hg38UCSC Ensembl
Innerchr22:34738070..34914075hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38176004
hg19176006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103086
Samplessample308
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116797
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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