A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097194



Internal ID21284235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98274705..98284323hg38UCSC Ensembl
Innerchr15:98817934..98827552hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg389619
hg199619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114672
Supporting Variants
Samplessample359
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097194
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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