A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585870



Internal ID21534418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42125912..42138063hg38UCSC Ensembl
chr22:42521917..42534072hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3812152
hg1912156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128192
SamplesHG03009
Known GenesCYP2D6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585870
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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