A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115109



Internal ID21298375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178139248..178143197hg38UCSC Ensembl
Innerchr3:177857036..177860985hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383950
hg193950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv828n145
Supporting Variantsnssv14108225
Samplessample218
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115109
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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