A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094803



Internal ID21285362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43266319..43272506hg38UCSC Ensembl
Innerchr4:43268336..43274523hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386188
hg196188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115217
Supporting Variants
Samplessample373
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094803
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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