A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956206



Internal ID22731398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28840756..29187756hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38347001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1288n209
Supporting Variantsnssv17407549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956206
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