A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551782



Internal ID20924915
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 StatusM
Merged Variantsdgv4711n223
Supporting Variantsnssv18074556
Samples
Known GenesCYP2D6, CYP2D7P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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