A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519362



Internal ID295713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51919423..51921784hg38UCSC Ensembl
chr20:50535962..50538323hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519362
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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