A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484606



Internal ID21142159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66108568..66146376hg38UCSC Ensembl
chr13:66682700..66720508hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3837809
hg1937809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484606
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