A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104261



Internal ID22013494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24438529..24438529hg38UCSC Ensembl
chr22:24834497..24834497hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641577
Samples
Known GenesADORA2A, ADORA2A-AS1, SPECC1L-ADORA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104261
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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