A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059103



Internal ID21968336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42566394..42674276hg38UCSC Ensembl
chr20:41195034..41302916hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38107883
hg19107883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627646
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059103
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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