A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094058



Internal ID21277324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:59394126..59400236hg38UCSC Ensembl
Innerchr14:59860844..59866954hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110918
Supporting Variants
Samplessample25
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094058
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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