A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519299



Internal ID295651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41031792..41031850hg38UCSC Ensembl
chr20:39660432..39660490hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725975
Samples
Known GenesTOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519299
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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