A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059321



Internal ID21968555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5938851..5938919hg38UCSC Ensembl
chr20:5919497..5919565hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635833
Samples
Known GenesTRMT6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059321
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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