A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459809



Internal ID237817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37659515..37660206hg38UCSC Ensembl
chr4:37661137..37661828hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947413
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459809
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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