A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729887



Internal ID153553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49929564..49959564hg38UCSC Ensembl
chr22:50323212..50353212hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3830001
hg1930001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729887
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.254545


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