A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524984



Internal ID20898345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:464234..489770hg38UCSC Ensembl
chr19:464234..489770hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3825537
hg1925537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198914
Samples
Known GenesODF3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524984
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