A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098139



Internal ID21286676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94838944..94846137hg38UCSC Ensembl
Innerchr15:95382173..95389366hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg387194
hg197194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116413
Supporting Variants
Samplessample392
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098139
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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