A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940618



Internal ID22716029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85974902..85980765hg38UCSC Ensembl
chr16:86008508..86014371hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385864
hg195864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940618
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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