A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045022



Internal ID21954292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34832702..34832852hg38UCSC Ensembl
chr22:35228693..35228843hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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