ID GM19214 AC CVCL_P551 DR CLO; CLO_0027255 DR ArrayExpress; E-GEUV-1 DR ArrayExpress; E-GEUV-2 DR ArrayExpress; E-GEUV-3 DR Coriell; GM19214 DR GEO; GSM649290 DR GEO; GSM1720159 DR IGSR; NA19214 DR Wikidata; Q54850289 RX PubMed=21397061; RX PubMed=24037378; RX PubMed=27617755; CC Part of: International Genome Sample Resource (1000 genomes project) cell lines. CC Population: African; Yoruba in Ibadan, Nigeria (YRI). CC Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV). CC Omics: Genomics; Whole genome sequencing. CC Omics: Transcriptomics; RNAseq. CC Omics: Variations; CNV analysis. CC Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Female AG Age unspecified CA Transformed cell line DT Created: 05-11-13; Last updated: 10-04-25; Version: 16 // RX PubMed=21397061; DOI=10.1016/j.ajhg.2011.02.004; PMCID=PMC3059424; RA Campbell C.D., Sampas N., Tsalenko A., Sudmant P.H., Kidd J.M., RA Malig M., Vu T.H., Vives L., Tsang P., Bruhn L., Eichler E.E.; RT "Population-genetic properties of differentiated human copy-number RT polymorphisms."; RL Am. J. Hum. Genet. 88:317-332(2011). // RX PubMed=24037378; DOI=10.1038/nature12531; PMCID=PMC3918453; RA Lappalainen T., Sammeth M., Friedlander M.R., 't Hoen P.A.C., RA Monlong J., Rivas M.A., Gonzalez-Porta M., Kurbatova N., Griebel T., RA Ferreira P.G., Barann M., Wieland T., Greger L., van Iterson M., RA Almlof J.C., Ribeca P., Pulyakhina I., Esser D., Giger T., Tikhonov A., RA Sultan M., Bertier G., MacArthur D.G., Lek M., Lizano E., RA Buermans H.P.J., Padioleau I., Schwarzmayr T., Karlberg O., Ongen H., RA Kilpinen H., Beltran S., Gut M., Kahlem K., Amstislavskiy V., RA Stegle O., Pirinen M., Montgomery S.B., Donnelly P., McCarthy M.I., RA Flicek P., Strom T.-M., Lehrach H., Schreiber S., Sudbrak R., RA Carracedo A., Antonarakis S.E., Hasler R., Syvanen A.-C., RA van Ommen G.-J.B., Brazma A., Meitinger T., Rosenstiel P., Guigo R., RA Gut I.G., Estivill X., Dermitzakis E.T.; RG Geuvadis Consortium; RT "Transcriptome and genome sequencing uncovers functional variation in RT humans."; RL Nature 501:506-511(2013). // RX PubMed=27617755; DOI=10.1038/srep32406; PMCID=PMC5019111; RA Ferreira P.G., Oti M., Barann M., Wieland T., Ezquina S., RA Friedlander M.R., Rivas M.A., Esteve-Codina A., Rosenstiel P., RA Strom T.-M., Lappalainen T., Guigo R., Sammeth M.; RG Geuvadis Consortium; RT "Sequence variation between 462 human individuals fine-tunes RT functional sites of RNA processing."; RL Sci. Rep. 6:32406-32406(2016). //