A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098668



Internal ID21287113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65053404..65058829hg38UCSC Ensembl
Innerchr17:63049522..63054947hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg385426
hg195426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117078
Supporting Variants
Samplessample397
Known GenesGNA13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098668
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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