A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045655



Internal ID21954919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64012429..64012542hg38UCSC Ensembl
chr20:62643782..62643895hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643414
Samples
Known GenesPRPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045655
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