A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099984



Internal ID21277138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:738668..769455hg38UCSC Ensembl
Innerchr20:719312..750099hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3830788
hg1930788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115526
Supporting Variants
Samplessample246
Known GenesSLC52A3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099984
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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