A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524087



Internal ID300298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56051909..56142850hg38UCSC Ensembl
chr20:54626965..54717906hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3890942
hg1990942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524087
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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