A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941574



Internal ID22717000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:355169..386913hg38UCSC Ensembl
chr20:335813..367557hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3831745
hg1931745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392096
Samples
Known GenesTRIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941574
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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