A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4702n223



Internal ID22807670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39030901..39052771hg38UCSC Ensembl
chr22:39426906..39448776hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3821871
hg1921871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6537874, nsv6540034
Samples
Known GenesAPOBEC3D, APOBEC3F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4702n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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