A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531087



Internal ID20904448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20161447..20166253hg38UCSC Ensembl
chr20:20142091..20146897hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384807
hg194807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205264
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531087
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