A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105616



Internal ID21288986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58746277..59058392hg38UCSC Ensembl
Innerchr3:58732004..59044118hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38312116
hg19312115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114115
Supporting Variants
Samplessample424
Known GenesC3orf67
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105616
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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