A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666460



Internal ID21614765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23268010..23268010hg38UCSC Ensembl
chr20:23248647..23248647hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116267
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666460
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