Hs04930970_cn

• Gene Symbol: DPY19L1P1
• Assay Reference Genome Location: Chr.7:32608499 on build GRCh38
• Cytoband: 7p14.3

Target Gene Details

• Entrez Gene ID: 100129460
• Gene Name: DPY19L1 pseudogene 1
• Gene Aliases: -
• Location: Chr.7:32580939-32719168 on Build GRCh38
• Assay Gene Location: Within Intron 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
DPY19L1P1	NR_036680.1
	AK026768.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv436557	Chr.7:30288062 - 32730902 on Build GRCh38	Deletion	PDE1C GHRHR MIR550A1 LOC401320 PPP1R17 MIR550B1 FAM188B GARS GGCT ZNRF2P1 AVL9 CCDC129 INMT-FAM188B CRHR2 DKFZP586I1420 DPY19L1P1 INMT LOC100130673 AQP1 LOC101928268 LSM5 NOD1 ADCYAP1R1 NEUROD6 LINC01176 ZNRF2

More Information

Additional Information:

For this assay, SNP(s) [rs67223828] 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