A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059868



Internal ID21969101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45879585..45879639hg38UCSC Ensembl
chr22:46275465..46275519hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059868
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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