A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701519



Internal ID21223344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45906710..45907145hg38UCSC Ensembl
chr20:44535349..44535784hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802254
Supporting Variants
Samples
Known GenesPLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701519
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.234375


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