A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111645



Internal ID21294911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20836840..20839639hg38UCSC Ensembl
Innerchr7:20876459..20879258hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085694
Samplessample417
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111645
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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