A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115786



Internal ID21299052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26288055..26292982hg38UCSC Ensembl
Innerchr4:26289677..26294604hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384928
hg194928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv867n145
Supporting Variantsnssv14096596, nssv14107369
Samplessample413, sample46
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115786
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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