A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094081



Internal ID21282651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58636713..58639786hg38UCSC Ensembl
Innerchr14:59103431..59106504hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383074
hg193074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114368
Supporting Variants
Samplessample33
Known GenesDACT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094081
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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