A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648343



Internal ID21840390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38189008..38189239hg38UCSC Ensembl
chr22:38585015..38585246hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648343
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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