A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071514



Internal ID20638554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41487492..41487994hg38UCSC Ensembl
chr21:42859419..42859921hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540425
Supporting Variants
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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