A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054058



Internal ID21963291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53489674..53494188hg38UCSC Ensembl
chr20:52106213..52110727hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384515
hg194515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619935
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054058
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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