A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365308



Internal ID21022861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52685401..52687600hg38UCSC Ensembl
chr3:52719417..52721616hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209992
Samples
Known GenesGNL3, PBRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365308
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