A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852514



Internal ID22627449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:460362..494484hg38UCSC Ensembl
chr8:410362..444484hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3834123
hg1934123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509243
Samples
Known GenesFBXO25, TDRP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852514
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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