A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089312



Internal ID21267368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:110046668..110076022hg38UCSC Ensembl
Innerchr4:110967824..110997178hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3829355
hg1929355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111663
Supporting Variants
Samplessample111
Known GenesELOVL6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089312
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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