A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618231



Internal ID21566536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39427684..39427684hg38UCSC Ensembl
chr3:39469175..39469175hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120842
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618231
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