Assay Details
Target Gene Details
Entrez Gene ID: | 2323 |
Gene Name: | fms related tyrosine kinase 3 ligand |
Gene Aliases: |
FL, FLT3L |
Location: |
Chr.19:49474172-49487038 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 3 - Intron 3 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss | SIGLEC11 TRPM4 PPP1R15A BSPH1 CGB3 PTOV1-AS1 SPHK2 PPFIA3 C19orf68 CD37 PLA2G4C-AS1 GFY NUCB1-AS1 MAMSTR BCAT2 FLJ26850 DHDH SYNGR4 MIR4751 TSKS SNAR-A14 C19orf73 PRMT1 PTOV1-AS2 GRIN2D RRAS BCL2L12 CARD8 PNKP LIG1 ALDH16A1 GYS1 SNAR-A6 CYTH2 HSD17B14 SNAR-C5 SNAR-A9 PRR12 SNAR-B1 NTN5 SNAR-A3 SNORD32A LHB LIN7B IRF3 ADM5 LOC101059948 AP2A1 SNAR-B2 SNAR-A5 SNAR-G1 BAX TULP2 DKKL1 GRWD1 LOC100287477 RPL18 VRK3 RUVBL2 SULT2B1 CABP5 MIR4749 PRRG2 SLC17A7 LMTK3 SLC6A16 SNRNP70 MIR4324 FTL MIR6799 EMP3 SNAR-C4 SNAR-A7 SEC1P SNAR-G2 SNAR-C2 ZNF473 CGB5 SIGLEC16 NTF4 SNORD35B SNAR-C3 SNAR-A1 CCDC155 RASIP1 PLEKHA4 PIH1D1 CGB2 FLT3LG NOSIP FUZ CGB7 ELSPBP1 RPL13A FUT1 KCNA7 RPS11 IZUMO1 FGF21 FAM83E SNAR-A11 MIR4750 TMEM143 MIR150 TBC1D17 SNORD33 CARD8-AS1 SNAR-A2 MED25 KDELR1 CGB8 LOC101928295 SNAR-C1 SCAF1 TEAD2 KCNJ14 DBP RCN3 SNAR-D IL4I1 SNORD34 LOC105372430 CCDC114 CA11 ZNF114 CPT1C SNAR-A4 SNAR-A13 MIR6798 AKT1S1 SPACA4 PLA2G4C HRC MIR6800 SNAR-A12 NUCB1 SNAR-A10 NUP62 PTOV1 FUT2 PTH2 SNORD35A LOC105447645 MIR5088 FCGRT ATF5 SNAR-A8 CGB1 |
nsv833862 | Chr.19:49448789 - 49570676 on Build GRCh38 | Loss | SNORD35B RPS11 SNORD32A RCN3 MIR150 SNORD34 SNORD33 SNORD35A PIH1D1 FLT3LG NOSIP ALDH16A1 FCGRT RPL13A |
esv3644624 | Chr.19:49461676 - 49475440 on Build GRCh38 | Gain | FLT3LG ALDH16A1 |
nsv953599 | Chr.19:49386444 - 49506743 on Build GRCh38 | Deletion | SNORD35B RPS11 SNORD32A LOC101928295 SLC17A7 CCDC155 MIR150 SNORD34 PTH2 SNORD33 SNORD35A PIH1D1 FLT3LG ALDH16A1 GFY RPL13A |
More Information
Additional Information:
For this assay, SNP(s) [rs75750998] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Non-exonic DGV Variation |