A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616906



Internal ID21565211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189214962..189214962hg38UCSC Ensembl
chr3:188932751..188932751hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123348
SamplesNA19239
Known GenesTPRG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616906
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