ClinGen CNVs Track Settings
 
Clinical Genome Resource (ClinGen) CNVs

Maximum display mode:       Reset to defaults   
Select views (Help):
Coverage ▾       CNVs      
 
Coverage Configuration
Type of graph: Graph configuration help
Track height: pixels (range: 16 to 128)
Data view scaling: Always include zero: 
Vertical viewing range: min:  max:   (range: 0 to 100)
Transform function:Transform data points by: 
Windowing function: Smoothing window:  pixels
Negate values:
Draw y indicator lines:at y = 0.0:    at y =
Select subtracks by evidence and class:
 All Evidence Curated  Submitted 
Class
Pathogenic 
Likely Pathogenic 
Uncertain 
Likely Benign 
Benign 
List subtracks: only selected/visible    all    ()
  Class↓1 Evidence↓2 views↓3   Track Name↓4  
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 Benign  Curated  CNVs  ClinGen CNVs: Curated Benign   Schema 
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 Benign  Submitted  CNVs  ClinGen CNVs: Benign   Schema 
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 Configure 		 Benign  Submitted  Coverage  ClinGen CNVs: Benign Gain Coverage   Schema 
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 Configure 		 Benign  Submitted  Coverage  ClinGen CNVs: Benign Loss Coverage   Schema 
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 Likely Benign  Submitted  CNVs  ClinGen CNVs: Uncertain: Likely Benign   Schema 
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 Likely Pathogenic  Submitted  CNVs  ClinGen CNVs: Uncertain: Likely Pathogenic   Schema 
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 Pathogenic  Curated  CNVs  ClinGen CNVs: Curated Pathogenic   Schema 
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 Pathogenic  Submitted  CNVs  ClinGen CNVs: Pathogenic   Schema 
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 Configure 		 Pathogenic  Submitted  Coverage  ClinGen CNVs: Pathogenic Gain Coverage   Schema 
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 Configure 		 Pathogenic  Submitted  Coverage  ClinGen CNVs: Pathogenic Loss Coverage   Schema 
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 Uncertain  Submitted  CNVs  ClinGen CNVs: Uncertain   Schema