A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087012



Internal ID21293059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43356934..43840023hg38UCSC Ensembl
Innerchr8:43212077..43695166hg19UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38483090
hg19483090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116455
Supporting Variants
Samplessample95
Known GenesPOTEA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087012
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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