A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434413



Internal ID213089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15640885..15641523hg38UCSC Ensembl
chr4:15642508..15643146hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945237
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434413
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