What is the best / standard place to get a full list of SNPs and their coordinates in hg38?
I downloaded the SNPsnap database, but just realized that those coordinates are in hg19.
I'm trying to figure out how many SNP sites exist in my targeted genome sequencing data.
Many thanks.
Thank you for your clear response, Kevin. I see that I can download the list in BED format, but there doesn't appear to be a file with all chromosomes; instead, there is one file per chromosome. Is there a reason why one can't download the full list in BED format?
@OP: Download all 00-All.vcf.gz (with all the variants), then convert vcf to bed using vcf2bed.
Good idea, @cpad0112. Enjoy your bank holiday Monday.
you too @kevin
Hello gaelgarcia,
having one file per chromomse have the advantage that you only need to download one smaller file of you investigate only a specific region.
If you need all informations in one file, you can concatenate the files to one after downloading.
fin swimmer
Yes, as per fin swimmer. Large datasets are typically made available on a per chromosome basis. The VCF version of dbSNP should contain all variants across all chromosomes, though (but it's a very large file > 10GB).
Great - thanks again.