Naar de inhoud
GET /v1/meta

Endpoint catalogue & notes

Probeer het live

10 gratis calls per dag — geen registratie, geen API-key. Loopt via de oanor-gateway.

Aangepaste headers (optioneel)
api.oanor.com/dbvar-api

Het werkt. Haal een API-key op en gebruik hem in je project.

Verkrijg een API-sleutel

Codefragmenten

curl "https://api.oanor.com/dbvar-api/v1/meta" \
  -H "x-oanor-key: oanor_test_..."
await fetch("https://api.oanor.com/dbvar-api/v1/meta", {
  headers: { "x-oanor-key": "oanor_test_..." }
});
$ch = curl_init("https://api.oanor.com/dbvar-api/v1/meta");
curl_setopt($ch, CURLOPT_HTTPHEADER, ["x-oanor-key: oanor_test_..."]);
curl_setopt($ch, CURLOPT_RETURNTRANSFER, true);
$out = curl_exec($ch);
import requests
requests.get(
    "https://api.oanor.com/dbvar-api/v1/meta",
    headers={"x-oanor-key": "oanor_test_..."}
)

Voorbeeldrespons

Een echte respons van dit endpoint, vastgelegd bij de laatste health check.

{
    "data": {
        "note": "dbVar is NCBI's archive of human genomic structural variation — structural variants (SVs) larger than ~50 bp: copy-number variants (CNVs), large deletions and duplications, insertions, inversions and translocations. /v1/search?gene=BRCA1 finds structural variants overlapping a gene (or use q= for free-text), returning each variant's dbVar accession (e.g. nsv7897183), the study it came from, variant type, organism, overlapping genes, GRCh38 genomic placement and clinical significance; /v1/variant?id=nsv7897183 returns a single variant's full record — placements on all assemblies (GRCh37 and GRCh38), variant type, genes, clinical significance, study type, methods and variant counts (you may also pass the numeric uid). Accessions look like nsv… (variant), nssv… (variant call) or nstd… (study). Data from NCBI dbVar (public domain). A structural-variation / CNV resource — distinct from clinical single-nucleotide variant interpretation (ClinVar), population allele frequencies (gnomAD) and trait associations (GWAS). Ideal for genomics, cytogenetics, rare-disease and bioinformatics tools.",
        "source": "NCBI dbVar — database of genomic structural variation (ncbi.nlm.nih.gov/dbvar)",
        "endpoints": [
            "/v1/search",
            "/v1/variant",
            "/v1/meta"
        ]
    },
    "meta": {
        "timestamp": "2026-06-01T23:41:01.124Z",
        "request_id": "91116d99-5379-4d8e-94db-373ca2ae4cb1"
    },
    "status": "ok",
    "message": "Meta retrieved",
    "success": true
}