Hs02218098_cn

• Gene Symbol: ATP6V0E2-AS1
• Assay Reference Genome Location: Chr.7:149867905 on build GRCh38
• Cytoband: 7q36.1

Target Gene Details

• Entrez Gene ID: 401431
• Gene Name: ATP6V0E2 antisense RNA 1
• Gene Aliases: -
• Location: Chr.7:149867694-149873862 on Build GRCh38
• Assay Gene Location: Within Exon 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ATP6V0E2-AS1	NR_027040.1	4	2858
	AW452405.1	1	227

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv8229	Chr.7:149852698 - 150185474 on Build GRCh38	Gain+Loss	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C LOC100134040
nsv1033095	Chr.7:149810995 - 150084783 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C SSPO LOC100134040
nsv521861	Chr.7:149761534 - 149885817 on Build GRCh38	Loss	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C SSPO ZNF467
esv2759571	Chr.7:149744501 - 150259326 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C SSPO LOC100134040 ZNF467
esv3615438	Chr.7:149790046 - 150039200 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C SSPO LOC100134040
esv3576480	Chr.7:149621871 - 150131598 on Build GRCh38	Gain	ZNF862 ATP6V0E2 KRBA1 ATP6V0E2-AS1 ACTR3C ZNF767P SSPO LOC100134040 ZNF467
nsv831184	Chr.7:149727744 - 149903004 on Build GRCh38	Gain	ZNF862 ATP6V0E2 KRBA1 ATP6V0E2-AS1 ACTR3C SSPO ZNF467
esv3891234	Chr.7:149854904 - 150009836 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C
nsv1029484	Chr.7:149842825 - 149902237 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C
nsv1161666	Chr.7:149855457 - 150116613 on Build GRCh38	Duplication	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C LOC100134040
nsv831185	Chr.7:149864016 - 150022570 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C
dgv6751n100	Chr.7:149855445 - 149998108 on Build GRCh38	Gain	ZNF862 ATP6V0E2 ATP6V0E2-AS1 ACTR3C

More Information

Additional Information:

For this assay, SNP(s) [rs117690098] 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