A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563453



Internal ID336387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45459164..45460722hg38UCSC Ensembl
chr20:44087804..44089362hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563453
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer