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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.

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DD1688
 
Resource Report
Resource Website 		ECACC Cat# 93122217, RRID:CVCL_9H03 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=93122217)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 93122217 ECACC:93122217,
Wikidata:Q54829917		 CVCL_9H03 2026-07-25 04:29:50 0
DD1709
 
Resource Report
Resource Website 		ECACC Cat# 94011410, RRID:CVCL_9H13 Homo sapiens (Human) Congenital cystic hygroma Karyotypic information: 69,XXX (ECACC=94011410)., Part of: ECACC chromosomal abnormality collection. Finite cell line Sex ambiguous ECACC 94011410 ECACC:94011410,
Wikidata:Q54829929		 CVCL_9H13 2026-07-25 04:29:50 0
DD1642
 
Resource Report
Resource Website 		ECACC Cat# 93120317, RRID:CVCL_9G84 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=93120317)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 93120317 ECACC:93120317,
Wikidata:Q54829897		 CVCL_9G84 2026-07-25 04:29:49 0
DD1640
 
Resource Report
Resource Website 		ECACC Cat# 93120315, RRID:CVCL_9G82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 93120315 ECACC:93120315,
Wikidata:Q54829895		 CVCL_9G82 2026-07-25 04:29:49 0
DD1721
 
Resource Report
Resource Website 		ECACC Cat# 94012133, RRID:CVCL_9H21 Homo sapiens (Human) Karyotypic information: 46,XY,t(4;18)(p13;q11)mat (ECACC=94012133)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94012133 ECACC:94012133,
Wikidata:Q54829937		 CVCL_9H21 2026-07-25 04:29:50 0
DD1669
 
Resource Report
Resource Website 		ECACC Cat# 93121708, RRID:CVCL_9G99 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;18) (ECACC=93121708)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93121708 ECACC:93121708,
Wikidata:Q54829912		 CVCL_9G99 2026-07-25 04:29:50 0
DD1707
 
Resource Report
Resource Website 		ECACC Cat# 94011320, RRID:CVCL_9H11 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94011320 ECACC:94011320,
Wikidata:Q54829927		 CVCL_9H11 2026-07-25 04:29:50 0
DD1697
 
Resource Report
Resource Website 		ECACC Cat# 94010711, RRID:CVCL_9H07 Homo sapiens (Human) Karyotypic information: 47,XXX (ECACC=94010711)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 94010711 ECACC:94010711,
Wikidata:Q54829923		 CVCL_9H07 2026-07-25 04:29:50 0
DD1654
 
Resource Report
Resource Website 		ECACC Cat# 93121050, RRID:CVCL_9G90 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 93121050 ECACC:93121050,
Wikidata:Q54829903		 CVCL_9G90 2026-07-25 04:29:49 0
DD1705
 
Resource Report
Resource Website 		ECACC Cat# 94011318, RRID:CVCL_9H09 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94011318 ECACC:94011318,
Wikidata:Q54829925		 CVCL_9H09 2026-07-25 04:29:50 0
DD1717
 
Resource Report
Resource Website 		ECACC Cat# 94012018, RRID:CVCL_9H18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94012018 ECACC:94012018,
Wikidata:Q54829934		 CVCL_9H18 2026-07-25 04:29:50 0
DD1656
 
Resource Report
Resource Website 		ECACC Cat# 93121404, RRID:CVCL_9G92 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93121404 ECACC:93121404,
Wikidata:Q54829905		 CVCL_9G92 2026-07-25 04:29:49 0
DD1645
 
Resource Report
Resource Website 		ECACC Cat# 93120689, RRID:CVCL_9G86 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93120689 ECACC:93120689,
Wikidata:Q54829899		 CVCL_9G86 2026-07-25 04:29:49 0
DD1691
 
Resource Report
Resource Website 		ECACC Cat# 93123002, RRID:CVCL_9H05 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93123002 ECACC:93123002,
Wikidata:Q54829921		 CVCL_9H05 2026-07-25 04:29:50 0
DD1732
 
Resource Report
Resource Website 		ECACC Cat# 94012811, RRID:CVCL_9H27 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94012811 ECACC:94012811,
Wikidata:Q54829943		 CVCL_9H27 2026-07-25 04:29:51 0
DD1674
 
Resource Report
Resource Website 		ECACC Cat# 93122001, RRID:CVCL_9H00 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93122001 ECACC:93122001,
Wikidata:Q54829913		 CVCL_9H00 2026-07-25 04:29:50 0
DD1632
 
Resource Report
Resource Website 		ECACC Cat# 93120210, RRID:CVCL_9G80 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93120210 ECACC:93120210,
Wikidata:Q54829893		 CVCL_9G80 2026-07-25 04:29:49 0
DD1648
 
Resource Report
Resource Website 		ECACC Cat# 931207124, RRID:CVCL_9G88 Homo sapiens (Human) 22q11.2 deletion syndrome Karyotypic information: 46,XX,del(22) (ECACC=931207124)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 931207124 ECACC:931207124,
Wikidata:Q54829901		 CVCL_9G88 2026-07-25 04:29:49 0
DD1637
 
Resource Report
Resource Website 		ECACC Cat# 93120305, RRID:CVCL_9G81 Homo sapiens (Human) Karyotypic information: 47,XY,+dic(15)(pter->q11::q11->pter)mat (ECACC=93120305)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93120305 ECACC:93120305,
Wikidata:Q54829894		 CVCL_9G81 2026-07-25 04:29:49 0
DD1646
 
Resource Report
Resource Website 		ECACC Cat# 93120690, RRID:CVCL_9G87 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93120690 ECACC:93120690,
Wikidata:Q54829900		 CVCL_9G87 2026-07-25 04:29:49 0

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