A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146666



Internal ID345871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38189069..38189176hg38UCSC Ensembl
chr22:38585076..38585183hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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