Earlier quoted context omitted.
> you can get a full human genome sequenced at high coverage for between 1000 and 3000 USD This is not a "full" human genome, but a collection of 150bp fragments that can be realigned to an existing human genome. You cannot take this and infer the whole diploid genome of the individual. There is a huge amount that will be missed, and all of our current knowledge is based on this gappy picture of what's going on in si…
I think you are not sufficiently recognising how much structural variation can be resolved from short reads. There is certainly some that can't but a large proportion can be with the right tools.
Most structural variation I've seen based on whole genome assemblies is not even classifiable into neat categories like "deletion" or "insertion". If you think that "most" things are detected with short reads then you are deluded by the dominant technology.