A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104217



Internal ID21283823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:187970078..187972740hg38UCSC Ensembl
Innerchr3:187687866..187690528hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117149
Supporting Variants
Samplessample35
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104217
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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