Thank you, Ram. I was wondering if these contigs can be replaced by chr1..chrY?
NC_000001.10
NC_000002.11
NC_000003.11
NC_000004.11
NC_000005.9
NC_000006.11
NC_000007.13
Hi All, I need to annotate a VCF file using dbSNP latest data for GRCh38. I am using annovar to annotate the VCF file. Can someone please guide me to the right location? I was looking at this ftp (https://ftp.ncbi.nih.gov/snp/organisms/) and then went to this: https://ftp.ncbi.nih.gov/snp/organisms/human_9606_b151_GRCh38p7/VCF/
That link has all different VCF files for version 151. I am not sure if this is the latest version (I saw somewhere 155 is the latest version). Can someone please guide me to the right file? Thanks in advance!
This is the directory you're looking for:
https://ftp.ncbi.nih.gov/snp/redesign/latest_release/VCF/
curl -s https://ftp.ncbi.nih.gov/snp/redesign/latest_release/VCF/GCF_000001405.39.gz | zcat | head
##fileformat=VCFv4.2
##fileDate=20210513
##source=dbSNP
##dbSNP_BUILD_ID=155
##reference=GRCh38.p13
##phasing=partial
##INFO=<ID=RS,Number=1,Type=Integer,Description="dbSNP ID (i.e. rs number)">
##INFO=<ID=GENEINFO,Number=1,Type=String,Description="Pairs each of gene symbol:gene id. The gene symbol and id are delimited by a colon (:) and each pair is delimited by a vertical bar (|). Does not include pseudogenes.">
##INFO=<ID=PSEUDOGENEINFO,Number=1,Type=String,Description="Pairs each of pseudogene symbol:gene id. The pseudogene symbol and id are delimited by a colon (:) and each pair is delimited by a vertical bar (|)">
##INFO=<ID=dbSNPBuildID,Number=1,Type=Integer,Description="First dbSNP Build for RS">
To find this, you needed to either trust the naming (latest_release/VCF) or read the readme: https://ftp.ncbi.nih.gov/snp/00readme.txt
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