A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516430



Internal ID292890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67683858..67689379hg38UCSC Ensembl
chr15:67976196..67981717hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385522
hg195522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702938
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516430
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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