A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113823



Internal ID21297089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:154521073..154532888hg38UCSC Ensembl
Innerchr4:155442225..155454040hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3811816
hg1911816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107163
Samplessample10
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113823
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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