A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116642



Internal ID21299908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13872573..13875034hg38UCSC Ensembl
Innerchr7:13912198..13914659hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382462
hg192462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084813
Samplessample42
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116642
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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