A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482518



Internal ID21140071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104382901..104391200hg38UCSC Ensembl
chr13:105035251..105043550hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1988n223
Supporting Variantsnssv18192330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482518
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer