A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117149



Internal ID21300415
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 StatusM
Merged Variants
Supporting Variantsnssv14104217
Samplessample35
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117149
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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