A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117905



Internal ID21301171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105612619..105622404hg38UCSC Ensembl
Innerchr4:106533776..106543561hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg389786
hg199786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107605
Samplessample86
Known GenesARHGEF38
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117905
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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