A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117780



Internal ID21301046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194773439..195115020hg38UCSC Ensembl
Innerchr2:195638163..195979744hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38341582
hg19341582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103238
Samplessample81
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117780
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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