A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643523



Internal ID21835570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42125965..42135344hg38UCSC Ensembl
chr22:42521970..42531353hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg389380
hg199384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048521
Supporting Variants
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643523
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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