Cellosaurus DD1620 (CVCL_9G76)
| Cell line name | DD1620 |
|---|---|
| Accession | CVCL_9G76 |
| Resource Identification Initiative | To cite this cell line use: DD1620 (RRID:CVCL_9G76) |
| Comments | Part of: ECACC chromosomal abnormality collection. Derived from site: In situ; Umbilical cord; UBERON=UBERON_0002331. Cell type: Fibroblast; CL=CL_0000057. |
| Disease | 22q11.2 deletion syndrome (NCIt: C2989) 22q11.2 deletion syndrome (ORDO: Orphanet_567) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 4D |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 93112927 |
| Encyclopedic resources | Wikidata; Q54829888 |
| Entry history | |
| Entry creation | 23-Feb-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |