A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111663



Internal ID21294929
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 StatusM
Merged Variants
Supporting Variantsnssv14089312
Samplessample111
Known GenesELOVL6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111663
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer