A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520473



Internal ID20893834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6746344..6747899hg38UCSC Ensembl
chr20:6726991..6728546hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381556
hg191556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer