A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633469



Internal ID21825516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55960640..55960953hg38UCSC Ensembl
chr20:54535696..54536009hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633469
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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