A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113438



Internal ID21296704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151386886..151412970hg38UCSC Ensembl
Innerchr5:150766447..150792531hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3826085
hg1926085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv996n145
Supporting Variantsnssv14097307, nssv14109243
Samplessample84, sample282
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113438
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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