A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060070



Internal ID21969303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24288952..24667424hg38UCSC Ensembl
chr22:24684920..25063391hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38378473
hg19378472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647583
Samples
Known GenesADORA2A, ADORA2A-AS1, BCRP3, FAM211B, GGT1, GUCD1, POM121L10P, SNRPD3, SPECC1L, SPECC1L-ADORA2A, UPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060070
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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