A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605861



Internal ID21554166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25783480..25783480hg38UCSC Ensembl
chr3:25824971..25824971hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123606
SamplesHG03065
Known GenesNGLY1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605861
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