A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069509



Internal ID20636549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18363324..18363895hg38UCSC Ensembl
chr21:19735641..19736212hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544288
Supporting Variants
Samples
Known GenesTMPRSS15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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