A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518359



Internal ID20891720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21298801..21305400hg38UCSC Ensembl
chr20:21279439..21286038hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203216
Samples
Known GenesXRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518359
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