A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726999



Internal ID150665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41506669..41527633hg38UCSC Ensembl
chr21:42878596..42899560hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3820965
hg1920965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534810
Supporting Variants
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726999
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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