A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108561



Internal ID21284255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58489474..58494225hg38UCSC Ensembl
Innerchr3:58475201..58479952hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg384752
hg194752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117229
Supporting Variants
Samplessample359
Known GenesKCTD6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108561
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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