A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060014



Internal ID21969248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63794205..63804635hg38UCSC Ensembl
chr20:62425558..62435988hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810431
hg1910431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644553
Samples
Known GenesZBTB46
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060014
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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