A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871880



Internal ID22646818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29311415..29325927hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3814513
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1300n209
Supporting Variantsnssv17483989, nssv17483990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871880
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