A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060030



Internal ID21969263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47590170..47590417hg38UCSC Ensembl
chr22:47985919..47986166hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060030
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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