A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533259



Internal ID309155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40835861..40835997hg38UCSC Ensembl
chr20:39464501..39464637hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533259
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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