For better experience, turn on JavaScript!



A tool for interpretation of copy number variation (CNV) in the context of topologically associated domains (TADs).


Genotype and phenotype; Transcription factors and regulatory sites; Genetic variation


  • Operation: Genotyping
  • Software interface: Web user interface
  • Language: Python
  • Operating system: Linux; Mac OS X; Microsoft Windows
  • License: Not stated
  • Cost: Free
  • Version name: -
  • Maturity: Stable
  • Credit: The UCSF Department of Laboratory Medicine (to JDS), a Clinical Scientist Development Award from the Doris Duke Charitable Foundation (to APW), and NIH Clinical Scientist Development Award K08CA184116 (to APW).
  • Contact: ClinicalTAD _at_
  • Collection: -


Spector JD, Wiita AP "ClinTAD: a tool for copy number variant interpretation in the context of topologically associated domains." J Hum Genet. 2019 May;64(5):437-443.
PMID: 30765865

Download and documentation

If you find errors, please report here.