A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643488



Internal ID21591793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128826785..128826785hg38UCSC Ensembl
chr10:130625049..130625049hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386091
hg196091
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066797
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643488
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