Hs01180679_cn

• Gene Symbol: CD164L2
• Assay Reference Genome Location: Chr.1:27381835 on build GRCh38
• Cytoband: 1p36.11

Target Gene Details

• Entrez Gene ID: 388611
• Gene Name: CD164 molecule like 2
• Gene Aliases: EAPG6122, UNQ6122
• Location: Chr.1:27379100-27383333 on Build GRCh38
• Assay Gene Location: Overlaps Intron 3 - Exon 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CD164L2	NM_207397.3			NP_997280.2
	XM_005245868.3			XP_005245925.2
	XM_011541441.1			XP_011539743.1
	AY358761.1			AAQ89121.1
	BC137466.1
	DB114521.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv526051	Chr.1:27284255 - 27445496 on Build GRCh38	Gain	MAP3K6 WDTC1 WASF2 CD164L2 SYTL1 ACTG1P20 FCN3 GPR3 TMEM222
nsv516766	Chr.1:27335744 - 27405147 on Build GRCh38	Loss	MAP3K6 WASF2 CD164L2 SYTL1 FCN3 GPR3 TMEM222

More Information

Additional Information:

For this assay, SNP(s) [rs76651420] 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