Hs03663545_cn

• Gene Symbol: LOC286059
• Assay Reference Genome Location: Chr.8:23081308 on build GRCh38
• Cytoband: 8p21.3

Target Gene Details

• Entrez Gene ID: 286059
• Gene Name: tumor necrosis factor receptor superfamily member 10d, decoy with truncated death domain pseudogene
• Gene Aliases: -
• Location: Chr.8:23068229-23083619 on Build GRCh38
• Assay Gene Location: Within Exon 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC286059	NR_038873.1	3	325
	AK024295.1	3	346

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv1027718	Chr.8:22805950 - 23258334 on Build GRCh38	Gain	LOC254896 TNFRSF10B RHOBTB2 LOC389641 PEBP4 CHMP7 LOC101929237 LOC286059 LOC107984124 TNFRSF10A TNFRSF10C TNFRSF10D
nsv1025672	Chr.8:22868571 - 23130480 on Build GRCh38	Gain	LOC254896 TNFRSF10B RHOBTB2 PEBP4 LOC101929237 LOC286059 LOC107984124 TNFRSF10C
nsv1015967	Chr.8:23056273 - 23105040 on Build GRCh38	Loss	LOC254896 TNFRSF10B LOC286059 TNFRSF10C
nsv610775	Chr.8:23080343 - 23139266 on Build GRCh38	Loss	LOC254896 LOC286059 TNFRSF10C TNFRSF10D
esv2759604	Chr.8:20675533 - 23254096 on Build GRCh38	Loss	POLR3D REEP4 XPO7 SLC39A14 EGR3 LOC286114 NUDT18 TNFRSF10B RHOBTB2 LOC101929237 LOC107986876 PDLIM2 LOC107984124 LOC102467222 NPM2 DOK2 LOC101929172 HR LOC254896 SORBS3 LGI3 FAM160B2 BIN3 DMTN BIN3-IT1 CHMP7 MIR320A FGF17 GFRA2 PIWIL2 TNFRSF10A TNFRSF10C PPP3CC SFTPC PHYHIP LOC389641 PEBP4 C8orf58 LOC286059 TNFRSF10D CCAR2 LOC100507071 BMP1
nsv1025279	Chr.8:23079697 - 23182344 on Build GRCh38	Loss	LOC254896 LOC286059 TNFRSF10C TNFRSF10D
dgv12057n54	Chr.8:23071837 - 23183569 on Build GRCh38	Loss	LOC254896 LOC286059 TNFRSF10C TNFRSF10D
esv2736750	Chr.8:23028863 - 23201144 on Build GRCh38	Deletion	LOC254896 TNFRSF10B LOC286059 TNFRSF10A TNFRSF10C TNFRSF10D
nsv1017570	Chr.8:22969562 - 23544783 on Build GRCh38	Gain	LOC254896 R3HCC1 CHMP7 TNFRSF10A TNFRSF10C TNFRSF10B RHOBTB2 LOC100507156 LOC389641 SLC25A37 LOXL2 LOC286059 LOC107984124 ENTPD4 TNFRSF10D
esv2736752	Chr.8:23072937 - 23106406 on Build GRCh38	Deletion	LOC254896 LOC286059 TNFRSF10C

More Information

Additional Information:

For this assay, SNP(s) [rs77529382] 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, Exonic, DGV Variation