A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113494



Internal ID21296760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62388980..62494266hg38UCSC Ensembl
Innerchr14:62855698..62960984hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38105287
hg19105287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093006
Samplessample1
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113494
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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