A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590716



Internal ID21539286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79419091..79419159hg38UCSC Ensembl
chr13:79993226..79993294hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079790
SamplesHG00731
Known GenesRBM26-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590716
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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