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Cellosaurus DD1620 (CVCL_9G76)

[Text version]
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 creation23-Feb-2016
Last entry update29-Jun-2023
Version number7