A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206842



Internal ID20773883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42128601..42139400hg38UCSC Ensembl
chr22:42524603..42535411hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3810800
hg1910809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536737
Supporting Variants
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00559


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