A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097759



Internal ID21278718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37486060..37492098hg38UCSC Ensembl
Innerchr17:35846166..35852204hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386039
hg196039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116169
Supporting Variants
Samplessample273
Known GenesDUSP14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097759
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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