A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528278



Internal ID20901639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50415935..50424617hg38UCSC Ensembl
chr19:50919192..50927874hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg388683
hg198683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198278
Samples
Known GenesPOLD1, SPIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528278
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