A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486290



Internal ID263659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97591877..97592279hg38UCSC Ensembl
chr10:99351634..99352036hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039767
Samples
Known GenesHOGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486290
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