A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524426



Internal ID20897787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21124401..21128500hg38UCSC Ensembl
chr20:21105042..21109141hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203213
Samples
Known GenesPLK1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524426
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