AutismKB 2.0

View CNVs/SVs


View by Evidence Type: All ( CNVs Only Present In Patients   de novo CNVs   Overlapping/Recurrent CNVs  
                                        CNVs Overlapping With ACRD   CNVs Not Present In Control   Significant Enriched CNVs   Others  All  )


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Notes: ACRD: Autism Chromosome Rearrangement Database
CNV Name Chr Band Gain/Loss Number of CNVs Evidence Type Reference
Case Control
AutCNV0005882 2 2q24.2 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005883 2 2q32.2 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005884 3 3p24.1 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005885 4 4p16.1 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005886 4 4q24 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005887 5 5q13.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005888 5 5q15 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005889 5 5q31.2 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005890 5 5q32 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005891 5 5q35.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005892 6 6q13 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005893 6 6q16.1 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005894 6 6q25.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005895 7 7q11.22 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005896 7 7q11.23 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005897 7 7q21.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005898 7 7q31.1 - - - de novo CNVs; Brandler WM, 2018
AutCNV0005899 7 7q34 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005900 8 8p23.2 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005901 8 8q12.1 loss - - Brandler WM, 2018
AutCNV0005902 8 8q24.3 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005903 9 9p23 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005904 9 9q21.31 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005905 9 9q22.31 loss - - Brandler WM, 2018
AutCNV0005906 9 9q31.2 loss - - de novo CNVs; Brandler WM, 2018

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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018