A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646458



Internal ID21838505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41475509..41475639hg38UCSC Ensembl
chr21:42847436..42847566hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043824
Supporting Variants
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646458
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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