A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110799



Internal ID21294065
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 StatusM
Merged Variants
Supporting Variantsnssv14093965
Samplessample289
Known GenesADCY4, LTB4R
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110799
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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