A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481509



Internal ID258985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16808100..16978218hg38UCSC Ensembl
chr10:16850099..17020217hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38170119
hg19170119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032504
Samples
Known GenesCUBN, RSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481509
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