A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642917



Internal ID21834964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42125962..42139826hg38UCSC Ensembl
chr22:42521967..42535837hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3813865
hg1913871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052872
Supporting Variants
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642917
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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