A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055841



Internal ID21965074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34821056..34823109hg38UCSC Ensembl
chr22:35217047..35219100hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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