A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878141



Internal ID22653105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46754079..46758702hg38UCSC Ensembl
chr20:45382718..45387341hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg384624
hg194624
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878141
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