A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666135



Internal ID21614440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119496996..119513594hg38UCSC Ensembl
chr8:120509236..120525834hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3816599
hg1916599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145201
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666135
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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