A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102786



Internal ID21267716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24421804..24438765hg38UCSC Ensembl
Innerchr22:24817772..24834733hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3816962
hg1916962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112574
Supporting Variants
Samplessample116
Known GenesADORA2A, ADORA2A-AS1, SPECC1L-ADORA2A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102786
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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