A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533487



Internal ID309376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60180405..60197562hg38UCSC Ensembl
chr20:58755463..58772620hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3817158
hg1917158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733413
Samples
Known GenesLOC284757
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533487
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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