A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649338



Internal ID21841385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18365520..18365749hg38UCSC Ensembl
chr21:19737837..19738066hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059031
Supporting Variants
Samples
Known GenesTMPRSS15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649338
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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