A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459716



Internal ID237726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184697358..184697426hg38UCSC Ensembl
chr4:185618512..185618580hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962230
Samples
Known GenesCENPU
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459716
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