A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097348



Internal ID21293096
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 StatusS
Merged Variantsnsv3115071
Supporting Variants
Samplessample96
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097348
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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