A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056451



Internal ID21965684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24423422..24423498hg38UCSC Ensembl
chr22:24819390..24819466hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639585
Samples
Known GenesSPECC1L-ADORA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056451
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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