A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059031



Internal ID21968264
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 StatusM
Merged Variants
Supporting Variantsnssv17649338
Samples
Known GenesTMPRSS15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059031
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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