A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096596



Internal ID21288210
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 StatusS
Merged Variantsnsv3115786
Supporting Variants
Samplessample413
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096596
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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