A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515488



Internal ID291969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10693589..10698409hg38UCSC Ensembl
chr20:10674237..10679057hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg384821
hg194821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515488
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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