Hs05371266_cn

• Gene Symbol: FAM174B
• Assay Reference Genome Location: Chr.15:92639270 on build GRCh38
• Cytoband: 15q26.1

Target Gene Details

• Entrez Gene ID: 400451
• Gene Name: family with sequence similarity 174 member B
• Gene Aliases: -
• Location: Chr.15:92617447-92734219 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM174B	NM_207446.2			NP_997329.2
	AK075564.1			BAC11703.1
	BC045729.1			AAH45729.1
	BC060873.1			AAH60873.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1674	Chr.15:92637781 - 92671702 on Build GRCh38	Insertion	LOC105370978 FAM174B
nsv1037972	Chr.15:92261678 - 92727531 on Build GRCh38	Loss	ST8SIA2 LOC105370978 LINC00930 C15orf32 FAM174B LOC104613533

More Information

Additional Information:

For this assay, SNP(s) [rs202189065] 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