A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4633n223



Internal ID22807601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18933001..19056500hg38UCSC Ensembl
chr22:18920514..19044013hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38123500
hg19123500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6554317, nsv6548729
Samples
Known GenesDGCR10, DGCR11, DGCR2, DGCR5, DGCR9, PRODH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4633n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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