A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117302



Internal ID21300568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48084471..48088869hg38UCSC Ensembl
Innerchr22:48480288..48484686hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg384399
hg194399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv738n145
Supporting Variantsnssv14103946
Samplessample385
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117302
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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