A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024003



Internal ID21933346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40623839..40630540hg38UCSC Ensembl
chr13:41197976..41204677hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg386702
hg196702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614529
Samples
Known GenesFOXO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024003
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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