Hs06190216_cn

• Gene Symbol: FAM183CP
• Assay Reference Genome Location: Chr.8:29924265 on build GRCh38
• Cytoband: 8p12

Target Gene Details

• Entrez Gene ID: 286135
• Gene Name: family with sequence similarity 183 member C, pseudogene
• Gene Aliases: -
• Location: Chr.8:29921513-29953609 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM183CP	NR_024473.1
	AL833525.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3616779	Chr.8:29919111 - 29925745 on Build GRCh38	Loss	FAM183CP

More Information

Additional Information:

For this assay, SNP(s) [rs77921327,rs80157577] 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, Intronic, Non-exonic, DGV Variation