A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880539



Internal ID22655509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80011774..80018954hg38UCSC Ensembl
chr18:77771774..77778954hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg387181
hg197181
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472516, nssv17479892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880539
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