A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613068



Internal ID21561373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98571698..98571698hg38UCSC Ensembl
chr3:98290542..98290542hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125126
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613068
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