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Cellosaurus DD1641 (CVCL_9G83)

[Text version]
Cell line name DD1641
Accession CVCL_9G83
Resource Identification Initiative To cite this cell line use: DD1641 (RRID:CVCL_9G83)
Comments Part of: ECACC chromosomal abnormality collection.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
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; 93120316
Encyclopedic resources Wikidata; Q54829896
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number7