A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661760



Internal ID21610065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129997440..129997440hg38UCSC Ensembl
chr11:129867335..129867335hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073509
SamplesNA19238
Known GenesPRDM10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661760
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