A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602886



Internal ID21551546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23176875..23374879hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38198005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084122
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602886
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