You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Hi, I can see that pathogenic structural variations come from Clinvar, but what are common and somatic types of SVs?
How to understand 'variant calls are from germline samples only (no somatic)'?
And how can I get the actual breakpoints of each structural variation? Is it possible to know whether identical variant calls were derived from different individuals or from the same sample but as a result of different analyses?
Thanks!
The text was updated successfully, but these errors were encountered:
Hi, I can see that pathogenic structural variations come from Clinvar, but what are common and somatic types of SVs?
How to understand 'variant calls are from germline samples only (no somatic)'?
And how can I get the actual breakpoints of each structural variation? Is it possible to know whether identical variant calls were derived from different individuals or from the same sample but as a result of different analyses?
Thanks!
The text was updated successfully, but these errors were encountered: