A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732977



Internal ID156643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52008896..52013668hg38UCSC Ensembl
chr20:50625435..50630207hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384773
hg194773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732977
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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