b7cb97d2942575d92f6385055e172dcbd979ee05 angie Tue Oct 1 13:09:29 2019 -0700 Adding new data type bigDbSnp.as with associated dbSnpDetails.as, for a track based on the new "dbSNP 2.0" schema and JSON downloads. refs #23283 diff --git src/hg/lib/bigDbSnp.as src/hg/lib/bigDbSnp.as new file mode 100644 index 0000000..17b3a4b --- /dev/null +++ src/hg/lib/bigDbSnp.as @@ -0,0 +1,21 @@ +table bigDbSnp +"Variant summary data extracted from dbSNP, 2019 and later" + ( + string chrom; "Reference sequence chromosome or scaffold" + uint chromStart; "Start position in chrom" + uint chromEnd; "End position in chrom" + string name; "dbSNP Reference SNP (rs) identifier" + lstring ref; "Reference allele; usually major allele, but may be minor allele" + int altCount; "Number of alternate alleles (usually 1)" + lstring[altCount] alts; "Alternate (non-reference) alleles; may include major allele" + uint shiftBases; "Bases by which an indel placement could be shifted left or right (display shows thin line over uncertain region, shifts minimal representation right)" + int freqSourceCount; "Number of projects reporting frequencies in current dbSNP build" + double[freqSourceCount] minorAlleleFreq; "Minor allele frequency, i.e. second highest allele frequency, from each frequency source; NaN if no data from project" + lstring[freqSourceCount] majorAllele; "Allele most frequently observed by each source" + lstring[freqSourceCount] minorAllele; "Allele second most frequently observed by each source" + uint maxFuncImpact; "Sequence Ontology (SO) ID number for greatest functional impact on gene; 0 if no SO terms are annotated" + enum(snv, mnv, ins, del, delins, identity) class; "Variation class/type" + lstring ucscNotes; "Interesting or anomalous properties noted by UCSC" + bigint _dataOffset; "Offset into bigDbSnpDetails file for line with more info" + int _dataLen; "Length of line in bigDbSnpDetails" + )