A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111814



Internal ID21295080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:195121804..195289247hg38UCSC Ensembl
Innerchr2:195986528..196153971hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38167444
hg19167444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103239
Samplessample81
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111814
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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