A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206838



Internal ID20773879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42125701..42129900hg38UCSC Ensembl
chr22:42521706..42525902hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg384200
hg194197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541771
Supporting Variants
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04025


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