A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4711n223



Internal ID22807679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42127556..42142900hg38UCSC Ensembl
chr22:42523558..42538901hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3815345
hg1915344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6548292, nsv6551782
Samples
Known GenesCYP2D6, CYP2D7P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4711n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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