A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206837



Internal ID20773878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42125201..42135000hg38UCSC Ensembl
chr22:42521206..42531006hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg389800
hg199801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551377
Supporting Variants
Samples
Known GenesCYP2D6, NDUFA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03234


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