A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552980



Internal ID20926095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42127201..42129800hg38UCSC Ensembl
chr22:42523203..42525802hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206840
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552980
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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