On Sunday, April 20th 2025, starting 8:30am GMT, there will be maintenance work that will involve the website being unavailable during parts of the day. We apologize for any inconvenience this may cause and appreciate your understanding.
We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Presentation outline
- Cataloging human genetic variation
- Spectrum of genetic variation
- Definitions
- Different types of variation databases
- The database of genomic variants (DGV)
- Aims of DGV
- History of the DGV
- What types of variants are in the database?
- Increase in variation data
- Current database content
- CNV distribution across the genome
- Who are the users of the database?
- Search options in the database
- Genome browser
- Tracks in the browser
- Detailed information page
- Data download
- Challenges in annotating structural variation
- CNV calls are relative to a reference
- Using a single sample as reference
- Using a population reference
- Using the assembly as reference (1)
- Using the assembly as reference (2)
- Reference: summary
- Boundaries
- Boundaries: clone based CGH
- Biases in current CNV annotations
- Boundaries: oligo arrays
- Merging regions
- CNVR and CNVE
- Complex regions
- Overview of databases
- DECIPHER
- How does DECIPHER work?
- Information about each syndrome
- Benefits and aims
- Chromosome anomaly collection
- ECARUCA
- dbRIP and dbSNP
- 1000 genomes project
- Archival databases
- Challenges going forward
- Acknowledgements
- Websites and references
Topics Covered
- Databases for CNV in control and disease populations
- Introduction to databases for capturing structural genetic variation
- An overview of the Database of Genomic Variants
- Challenges in annotating structural variation in light of imprecise data
- Rapid technology development
- Terminology used in the field
- Biases in existing data
- Overview of existing databases for copy number variation
Talk Citation
Feuk, L. (2009, August 30). Databases for CNV in control and disease populations [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 15, 2025, from https://doi.org/10.69645/AHRB2963.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Lars Feuk has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.