Hs04022404_cn

• Gene Symbol: VSTM2B
• Assay Reference Genome Location: Chr.19:29539310 on build GRCh38
• Cytoband: 19q12

Target Gene Details

• Entrez Gene ID: 342865
• Gene Name: V-set and transmembrane domain containing 2B
• Gene Aliases: -
• Location: Chr.19:29525431-29564555 on Build GRCh38
• Assay Gene Location: Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
VSTM2B	NM_001146339.1			NP_001139811.1
	XM_005258856.3			XP_005258913.1
	XM_011526902.2			XP_011525204.1
	XM_011526903.2			XP_011525205.1
	XM_011526904.2			XP_011525206.1
	XM_011526905.2			XP_011525207.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833798	Chr.19:29379175 - 29551378 on Build GRCh38	Loss	VSTM2B LOC284395
nsv1061604	Chr.19:28373028 - 29773397 on Build GRCh38	Loss	LOC101927210 VSTM2B LOC284395 LOC102724908 LOC102724958 PLEKHF1 UQCRFS1 LOC100420587 LINC00906 LINC01532 C19orf12 POP4

More Information

Additional Information:

For this assay, SNP(s) [rs77503640] 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 -

immunoglobulin receptor superfamily