A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662720



Internal ID21611025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128695049..128695049hg38UCSC Ensembl
chr11:128564944..128564944hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072947
SamplesNA19650
Known GenesFLI1, SENCR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662720
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