A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728078



Internal ID151744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24438480..24438556hg38UCSC Ensembl
chr22:24834448..24834524hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538313
Supporting Variants
Samples
Known GenesADORA2A, ADORA2A-AS1, SPECC1L-ADORA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728078
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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