A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544422



Internal ID20917662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42126401..42134700hg38UCSC Ensembl
chr22:42522403..42530706hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg388300
hg198304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4710n223
Supporting Variantsnssv18206839
Samples
Known GenesCYP2D6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544422
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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