Hs04056434_cn

• Gene Symbol: SIRPB2
• Assay Reference Genome Location: Chr.20:1489597 on build GRCh38
• Cytoband: 20p13

Target Gene Details

• Entrez Gene ID: 284759
• Gene Name: signal regulatory protein beta 2
• Gene Aliases: PTPN1L, PTPNS1L3, dJ776F14.2
• Location: Chr.20:1474591-1491762 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SIRPB2	NM_001122962.1			NP_001116434.1
	NM_001134836.1			NP_001128308.1
	XM_005260708.4			XP_005260765.1
	XM_005260709.3			XP_005260766.1
	XM_011529223.2			XP_011527525.1
	AK095499.1
	AK294440.1
	AK297072.1
	AY424277.1			AAR04783.1
	BM285394.1
	BQ635335.1
	DC313096.1
	DC358609.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv522008	Chr.20:1359746 - 1657932 on Build GRCh38	Gain	SDCBP2-AS1 FKBP1A MIR6869 FKBP1A-SDCBP2 SIRPD SIRPG-AS1 NSFL1C SIRPB1 SIRPB2 SIRPG
nsv833893	Chr.20:1433971 - 1547133 on Build GRCh38	Loss	SIRPD NSFL1C SIRPB2
nsv585206	Chr.20:1405829 - 1733716 on Build GRCh38	Gain	SIRPD SIRPG-AS1 NSFL1C SIRPB1 SIRPB2 SIRPG
nsv952971	Chr.20:1483656 - 1497554 on Build GRCh38	Duplication	SIRPB2

More Information

Additional Information:

For this assay, SNP(s) [rs80021678] 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

Panther Classification:

Molecular Function -

transmembrane signal receptor