A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536737



Internal ID20910080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42128601..42139400hg38UCSC Ensembl
chr22:42524603..42535411hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3810800
hg1910809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206842
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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