A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113123



Internal ID21296389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186724934..186727672hg38UCSC Ensembl
Innerchr4:187646088..187648826hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg382739
hg192739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089446
Samplessample136
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113123
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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