ID   H7.s6-GFP
AC   CVCL_A5KW
SY   H7v1,12,17q,20q-GFP
DR   Wikidata; Q107115221
RX   PubMed=27829140;
CC   Characteristics: Aneuploid WA07 subline with gain of chromosome 1 that has an interstitial deletion at 1p22, gain of chromosome 17q, trisomy chromosome 12 and gain of copy number variant 20q11.21 (PubMed=27829140).
CC   Karyotypic information: 48,XX,+del(1)(p22;p22),der(6)t(6;17)(q27;q1),+12,ish dup(q11.21;q11.21) (PubMed=27829140).
CC   Genetic integration: Method=Transfection; Gene=FPbase; R9NL8; eGFP (Note=Enhanced GFP).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_S799 ! H7.s6
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 20-05-21; Last updated: 19-12-24; Version: 6
//
RX   PubMed=27829140; DOI=10.1016/j.stemcr.2016.10.003; PMCID=PMC5106530;
RA   Baker D.E.C., Hirst A.J., Gokhale P.J., Juarez M.A., Williams S.,
RA   Wheeler M., Bean K., Allison T.F., Moore H.D., Andrews P.W.,
RA   Barbaric I.;
RT   "Detecting genetic mosaicism in cultures of human pluripotent stem
RT   cells.";
RL   Stem Cell Reports 7:998-1012(2016).
//