A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399789



Internal ID22457659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45909234..45909408hg38UCSC Ensembl
chr20:44537873..44538047hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965502
Supporting Variants
Samples
Known GenesPLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399789
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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