A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046258



Internal ID21955503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63886510..63886793hg38UCSC Ensembl
chr20:62517863..62518146hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640648
Samples
Known GenesTPD52L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046258
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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