A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116228



Internal ID21299494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33312575..33334520hg38UCSC Ensembl
Innerchr4:33314197..33336142hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3821946
hg1921946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092134, nssv14092081
Samplessample218, sample207
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116228
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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