A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074556



Internal ID20641596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42128801..42142900hg38UCSC Ensembl
chr22:42524803..42538901hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3814100
hg1914099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551782
Supporting Variants
Samples
Known GenesCYP2D6, CYP2D7P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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