Hs07498835_cn

• Gene Symbol: LOC146880
• Assay Reference Genome Location: Chr.17:64750685 on build GRCh38
• Cytoband: 17q24.1

Target Gene Details

• Entrez Gene ID: 146880
• Gene Name: Rho GTPase activating protein 27 pseudogene
• Gene Aliases: -
• Location: Chr.17:64749662-64781999 on Build GRCh38
• Assay Gene Location: Within Exon 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC146880	NR_026899.1	12	2424
	AK055342.1	11	2295

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1066765	Chr.17:64520760 - 65128185 on Build GRCh38	Gain	LRRC37A3 AMZ2P1 LOC100507002 PLEKHM1P1 SMURF2 GNA13 CEP95 LOC146880 MIR4315-2 MIR6080
dgv3274n100	Chr.17:64618099 - 64978067 on Build GRCh38	Gain	LRRC37A3 AMZ2P1 PLEKHM1P1 SMURF2 LOC146880 MIR4315-2 MIR6080
nsv469875	Chr.17:64741770 - 64944984 on Build GRCh38	Loss	LRRC37A3 PLEKHM1P1 LOC146880 MIR4315-2 MIR6080
dgv44n68	Chr.17:64726315 - 64900956 on Build GRCh38	Loss	LRRC37A3 PLEKHM1P1 LOC146880 MIR4315-2 MIR6080
nsv960140	Chr.17:64749454 - 64758635 on Build GRCh38	Duplication	LOC146880

More Information

Additional Information:

For this assay, SNP(s) [rs114194846] 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