A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520710



Internal ID20894071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5804935..5854628hg38UCSC Ensembl
chr20:5785581..5835274hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3849694
hg1949694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203332
Samples
Known GenesC20orf196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520710
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