Is counting of each SNP position starts from the beginning of each chromosome? Or it is continuous?
For example
In my dataset first snp for chromosome 2 rs2685230 has a position 437664 and last SNP rs10191556 has a position 242521405
But first SNP at chromosome 13 rs11617984 has a position 19622143
Is this a mistake in my data, or it means that 13 chromosome has a first SNP at 19622143? Is it supposed to be shorter than chromosome 2?
So on a chromosome where is nucleotide number 0 or number 1. Is it on the very tip of the telomere? Is is the p telomere or the q arm telomere? So does the chromosomal position simply step up by 1 for each nucleotide marching through the centromere to the other arm?
The first base is at one of the ends (assuming non-circular DNA). Which of the two ends isn't always known. For mouse/human/etc. (i.e., high quality reference genomes), the first base is the tip of the p-arm. Yes, each subsequent base is one position higher.