Hs01965503_cn

• Gene Symbol: IGSF22
• Assay Reference Genome Location: Chr.11:18718683 on build GRCh38
• Cytoband: 11p15.1

Target Gene Details

• Entrez Gene ID: 283284
• Gene Name: immunoglobulin superfamily member 22
• Gene Aliases: IGFN2
• Location: Chr.11:18704305-18726939 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
IGSF22	NM_173588.3	8	932	NP_775859.3
	XM_011520030.2	6	3836	XP_011518332.1
	XM_011520031.2	6	3836	XP_011518333.1
	XM_017017607.1	7	3727	XP_016873096.1
	XM_017017608.1	7	1750	XP_016873097.1
	AK095113.1	8	932	BAC04488.1
	BC115397.1	8	883

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1047371	Chr.11:18709926 - 18741490 on Build GRCh38	Gain	IGSF22 PTPN5
nsv553633	Chr.11:18290154 - 19036904 on Build GRCh38	Gain	UEVLD GTF2H1 LDHAL6A PTPN5 TMEM86A TSG101 LDHA SPTY2D1 IGSF22 HPS5 MIR3159 LDHC MRGPRX1 SPTY2D1-AS1
nsv525192	Chr.11:18701244 - 18771813 on Build GRCh38	Loss	TMEM86A IGSF22 PTPN5
nsv525452	Chr.11:18714400 - 18780956 on Build GRCh38	Gain	IGSF22 PTPN5

More Information

Additional Information:

For this assay, SNP(s) [rs73428416] 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