A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113708



Internal ID21296974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26287955..26294888hg38UCSC Ensembl
Innerchr4:26289577..26296510hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg386934
hg196934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv868n145
Supporting Variantsnssv14094764, nssv14107280, nssv14089366
Samplessample369, sample120, sample32
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113708
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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