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Research tool·clinical·progenetix
Progenetix Cnv Search
Search for cancer biosamples with copy number variations (CNVs) in a specific genomic region. Combines disease filter with genomic coordinates to find samples with amplifications or deletions in genes of interest. Uses RefSeq chromosome accessions for coordinates. Example: searching for EGFR amplifications (refseq:NC_000007.14:55019017-55211628, DUP) in breast cancer (NCIT:C4017) returns 9 matching biosamples.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
View JSON schemaExpandCollapse
JSON · 39 lines · 1,177 chars
Examples (1)
Default Progenetix Cnv Search call
Public-safe example · rate-limited
JSON input · 6 lines · 86 chars
Expected response keys: success
Identifiers
- Catalog ID
- tu_Progenetix_cnv_search
- Tool name
- Progenetix_cnv_search
- Added
- 2026-05-01 00:58Z
- Tags
- tooluniverse