A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115362



Internal ID21298628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49751911..49889049hg38UCSC Ensembl
Innerchr13:50326047..50463185hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38137139
hg19137139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094377
Samplessample42
Known GenesKPNA3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115362
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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