A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047671



Internal ID21956905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45906723..45907158hg38UCSC Ensembl
chr20:44535362..44535797hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618047
Samples
Known GenesPLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047671
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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