A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483994



Internal ID261417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99603554..99604407hg38UCSC Ensembl
chr10:101363311..101364164hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483994
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