A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627646



Internal ID21819693
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 StatusS
Merged Variantsnsv6059103
Supporting Variants
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627646
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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