A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056951



Internal ID21966187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64017369..64017503hg38UCSC Ensembl
chr20:62648722..62648856hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639354
Samples
Known GenesPRPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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