A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100659



Internal ID21279604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55470841..55473950hg38UCSC Ensembl
Innerchr20:54087379..54090488hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg383110
hg193110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112863
Supporting Variants
Samplessample286
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100659
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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