A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882666



Internal ID22657643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29309933..29319502hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389570
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1299n209
Supporting Variantsnssv17483986, nssv17483985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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