Hs02619064_cn

• Gene Symbol: SEZ6L2
• Assay Reference Genome Location: Chr.16:29871612 on build GRCh38
• Cytoband: 16p11.2

Target Gene Details

• Entrez Gene ID: 26470
• Gene Name: seizure related 6 homolog like 2
• Gene Aliases: BSRPA, PSK-1
• Location: Chr.16:29871159-29899573 on Build GRCh38
• Assay Gene Location: Within Exon 18

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SEZ6L2	NM_001114099.2	17	2855	NP_001107571.1
	NM_001114100.2	16	2762	NP_001107572.1
	NM_001243332.1	18	3104	NP_001230261.1
	NM_001243333.1	17	2972	NP_001230262.1
	NM_012410.3	18	2894	NP_036542.1
	NM_201575.3	17	3065	NP_963869.2
	XM_005255252.2	17	2912	XP_005255309.1
	XM_017023135.1	16	2861	XP_016878624.1
	AB105376.1	18	2733
	AF131749.1	10	1625
	AJ245820.1	18	2733	CAB57950.1
	AJ245821.1	18	2733	CAB57951.1
	AJ245822.1	17	2694	CAB57952.1
	AK027407.1	16	2374
	AK027676.1	15	2344
	AK074998.1	14	2062	BAC11345.1
	AK293675.1	17	2817
	AY358404.1	17	3054	AAQ88770.1
	BC000567.2	16	2562	AAH00567.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv571818	Chr.16:29861040 - 29874126 on Build GRCh38	Loss	CDIPT-AS1 CDIPT SEZ6L2

More Information

Additional Information:

For this assay, SNP(s) [rs77367192] 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