A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648806



Internal ID21840853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41473949..41474748hg38UCSC Ensembl
chr21:42845876..42846675hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042329
Supporting Variants
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648806
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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