A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115718



Internal ID21298984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20083142..20111282hg38UCSC Ensembl
Innerchr5:20083251..20111391hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3828141
hg1928141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097413
Samplessample111
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115718
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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