A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096176



Internal ID21270705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73814719..73846372hg38UCSC Ensembl
Innerchr15:74107060..74138713hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3831654
hg1931654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114261
Supporting Variants
Samplessample154
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096176
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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