A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095283



Internal ID21292557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93407454..93456499hg38UCSC Ensembl
Innerchr15:93950683..93999728hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3849046
hg1949046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115040
Supporting Variants
Samplessample9
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095283
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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