Hs03970265_cn

• Gene Symbol: CCDC92B
• Assay Reference Genome Location: Chr.17:2748409 on build GRCh38
• Cytoband: 17p13.3

Target Gene Details

• Entrez Gene ID: 101928991
• Gene Name: coiled-coil domain containing 92B
• Gene Aliases: -
• Location: Chr.17:2720801-2748500 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC92B	XM_017025489.1			XP_016880978.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1065489	Chr.17:2631416 - 3948349 on Build GRCh38	Gain	OR1E1 MIR6776 OR1D5 OR3A2 ATP2A3 OR1D2 OR3A1 CLUH OR1E2 GSG2 TAX1BP3 P2RX1 OR1D4 LOC101927911 TRPV1 LOC105371591 OR1G1 CAMKK1 OR1A2 LOC105371592 MIR1253 RAP1GAP2 OR3A3 OR1A1 OR3A4P ITGAE EMC6 PAFAH1B1 P2RX5 NCBP3 P2RX5-TAX1BP3 ASPA SHPK CTNS SPATA22 CCDC92B TRPV3
nsv833340	Chr.17:2705367 - 2783502 on Build GRCh38	Gain+Loss	LOC105371592 MIR1253 RAP1GAP2 LOC105371591 CLUH CCDC92B
nsv574225	Chr.17:2694675 - 2764987 on Build GRCh38	Loss	LOC105371592 MIR1253 RAP1GAP2 LOC105371591 CLUH CCDC92B
esv2660206	Chr.17:2679367 - 3519614 on Build GRCh38	Deletion	OR1E1 LOC105371592 MIR6776 MIR1253 OR1D5 OR3A2 RAP1GAP2 OR3A3 OR1A1 OR1D2 OR3A4P OR3A1 CLUH OR1E2 PAFAH1B1 ASPA OR1D4 LOC101927911 SPATA22 LOC105371591 OR1G1 CCDC92B TRPV3 OR1A2
nsv833339	Chr.17:2578764 - 2769775 on Build GRCh38	Loss	LOC105371592 MIR6776 MIR1253 RAP1GAP2 LOC105371591 CLUH CCDC92B PAFAH1B1

More Information

Additional Information:

For this assay, SNP(s) [rs576971712] 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