Could someone explain exactly what it means to be "completely sequence" the human genome when all humans have distinct genetic makeup (ie, different sequences of nucleobases in their DNA/RNA)?
While you are correct, the differences between different people's DNA is tiny, less 1% at best. So this information is still very valuable. This article is talking about the first time in finishing sequencing one person's Y chromosome's DNA.
How do we know this, if we have only sequenced the chromosome of one individual?