A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518859



Internal ID295223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10701587..10702429hg38UCSC Ensembl
chr20:10682235..10683077hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518859
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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