A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649418



Internal ID21597723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112761616..112761616hg38UCSC Ensembl
chr13:113415930..113415930hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080181
SamplesHG02818
Known GenesATP11A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649418
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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