A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110222



Internal ID21293488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:72993030..73021384hg38UCSC Ensembl
Innerchr4:73858747..73887101hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3828355
hg1928355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107217
Samplessample21
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110222
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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