A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926103



Internal ID18143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223320336..223325800hg38UCSC Ensembl
chr2:224185054..224190518hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg385465
hg195465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926103
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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