A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859642



Internal ID22634577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72420347..72424646hg38UCSC Ensembl
chr15:72712688..72716987hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859642
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