A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652613



Internal ID21600918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1766441..1766441hg38UCSC Ensembl
chr19:1766440..1766440hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103400
SamplesNA24385
Known GenesONECUT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652613
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