A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116511



Internal ID21299777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178139908..178143197hg38UCSC Ensembl
Innerchr3:177857696..177860985hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383290
hg193290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv828n145
Supporting Variantsnssv14108103, nssv14104310, nssv14105492, nssv14104540
Samplessample196, sample50, sample400, sample89
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116511
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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