This service allows the user to query information about variants on a certain chromosome at a certain location.
Usage
get_variant_by_location(
start,
end,
chromosome,
sortBy = "pos",
sortDirection = "asc",
page = 0,
itemsPerPage = 250
)
Arguments
- start
Integer.
- end
Integer.
- chromosome
String. One of "chr1", "chr2", "chr3", "chr4", "chr5", "chr6", "chr7", "chr8", "chr9", "chr10", "chr11", "chr12", "chr13", "chr14", "chr15", "chr16", "chr17", "chr18", "chr19", "chr20", "chr21", "chr22", "chrM", "chrX", "chrY".
- sortBy
String. Options: "sampleId", "ischemicTime", "aliquotId", "tissueSampleId", "hardyScale", "pathologyNotes", "ageBracket", "tissueSiteDetailId", "sex".
- sortDirection
String. Options: "asc", "desc". Default = "asc".
- page
Integer (default = 0).
- itemsPerPage
Integer (default = 250).
See also
Other Datasets Endpoints:
get_annotation()
,
get_collapsed_gene_model_exon()
,
get_downloads_page_data()
,
get_file_list()
,
get_full_get_collapsed_gene_model_exon()
,
get_functional_annotation()
,
get_linkage_disequilibrium_by_variant_data()
,
get_linkage_disequilibrium_data()
,
get_sample_datasets_endpoints()
,
get_subject()
,
get_tissue_site_detail()
,
get_variant()
Examples
get_variant_by_location(start = 153209600,
end = 153209700,
chromosome = "chr1")
#>
#> ── Paging info ─────────────────────────────────────────────────────────────────
#> • numberOfPages = 1
#> • page = 0
#> • maxItemsPerPage = 250
#> • totalNumberOfItems = 4
#> # A tibble: 4 × 10
#> snpId b37VariantId pos maf01 variantId alt chromosome snpIdUpper
#> <chr> <chr> <int> <lgl> <chr> <chr> <chr> <chr>
#> 1 rs11205220 1_153182115_T_… 1.53e8 TRUE chr1_153… C chr1 RS11205220
#> 2 rs1410858 1_153182116_C_… 1.53e8 TRUE chr1_153… A chr1 RS1410858
#> 3 rs139296761 1_153182120_C_… 1.53e8 FALSE chr1_153… T chr1 RS1392967…
#> 4 rs80104092 1_153182149_T_… 1.53e8 FALSE chr1_153… C chr1 RS80104092
#> # ℹ 2 more variables: datasetId <chr>, ref <chr>