A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518565



Internal ID20891926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:733010..809618hg38UCSC Ensembl
chr20:713654..790261hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3876609
hg1976608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204078
Samples
Known GenesSLC52A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518565
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