A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651866



Internal ID21600171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79020307..79020307hg38UCSC Ensembl
chr11:78731352..78731352hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076788
SamplesHG00513
Known GenesTENM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651866
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