Description:
INVERTED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
White
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XY,inv(10)(pter>p11::q21>p11::q21> qter)pat
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
7 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 10: INVERSION Breakpoint 10p11 inv(10)10p11 |
|
Chromosome 10: INVERSION Breakpoint 10q21 inv(10)10q21 |
Remarks |
Congenital malformations |
de la Chapelle A, Schroder J, Stenstrand K, Fellman J, Herva R, Saarni M, Anttolainen I, Tallila I, Tervila L, Husa L, Tallqvist G, Robson EB, Cook PJ, Sanger R, Pericentric inversions of human chromosomes 9 and 10. Am J Hum Genet26:746-66 1974 |
PubMed ID: 4140690 |
Passage Frozen |
7 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
|
|