A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093965



Internal ID21279738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24317098..24318748hg38UCSC Ensembl
Innerchr14:24786304..24787954hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381651
hg191651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110799
Supporting Variants
Samplessample289
Known GenesADCY4, LTB4R
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093965
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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