A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093987



Internal ID21280354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58634735..58640733hg38UCSC Ensembl
Innerchr14:59101453..59107451hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385999
hg195999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117362
Supporting Variants
Samplessample296
Known GenesDACT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093987
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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