A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128192



Internal ID21462755
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 StatusS
Merged Variantsnsv5585870
Supporting Variants
SamplesHG03009
Known GenesCYP2D6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128192
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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