A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053646



Internal ID21962879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17147492..17147544hg38UCSC Ensembl
chr22:17628382..17628434hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647746
Samples
Known GenesCECR5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053646
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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