A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115071



Internal ID21298337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103398540..103478460hg38UCSC Ensembl
Innerchr5:102734241..102814161hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3879921
hg1979921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097348
Samplessample96
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115071
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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