A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646133



Internal ID21594438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44490038..44490038hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105271
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646133
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