A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589437



Internal ID21538001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59819744..59819793hg38UCSC Ensembl
chr20:58394799..58394848hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117507
SamplesHG03486
Known GenesPHACTR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589437
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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