A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365015



Internal ID21022568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5174512..5344847hg38UCSC Ensembl
chr3:5216197..5386532hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38170336
hg19170336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209976
Samples
Known GenesARL8B, EDEM1, MIR4790
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365015
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