Hs03948105_cn

• Gene Symbol: LOC283922
• Assay Reference Genome Location: Chr.16:74340151 on build GRCh38
• Cytoband: 16q23.1

Target Gene Details

• Entrez Gene ID: 283922
• Gene Name: pyruvate dehydrogenase phosphatase regulatory subunit pseudogene
• Gene Aliases: -
• Location: Chr.16:74332406-74368255 on Build GRCh38
• Assay Gene Location: Within Intron 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC283922	NR_026950.1
	AK096768.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv32572	Chr.16:74340173 - 74421391 on Build GRCh38	Gain	LOC105376772 NPIPB15 LOC440386 LOC283922 CLEC18B
nsv9457	Chr.16:74326758 - 74431248 on Build GRCh38	Gain+Loss	LOC105376772 NPIPB15 LOC440386 LOC283922 CLEC18B
esv3639060	Chr.16:74315642 - 74364792 on Build GRCh38	Loss	LOC283922
esv3571520	Chr.16:74305225 - 74432521 on Build GRCh38	Gain	LOC105376772 PSMD7 NPIPB15 LOC440386 LOC283922 CLEC18B
esv2762054	Chr.16:74303138 - 74473158 on Build GRCh38	Gain	LOC105376772 PSMD7 NPIPB15 LOC440386 LOC283922 GLG1 CLEC18B
nsv833277	Chr.16:74300889 - 74464235 on Build GRCh38	Loss	LOC105376772 PSMD7 NPIPB15 LOC440386 LOC283922 GLG1 CLEC18B
nsv1065964	Chr.16:74054192 - 74541706 on Build GRCh38	Gain	LOC105376772 PSMD7 NPIPB15 LOC440386 LOC283922 GLG1 CLEC18B LOC101928035
esv3553661	Chr.16:74325697 - 74370953 on Build GRCh38	Deletion	LOC440386 LOC283922
nsv827736	Chr.16:74303148 - 74430368 on Build GRCh38	Gain	LOC105376772 PSMD7 NPIPB15 LOC440386 LOC283922 CLEC18B
esv3639061	Chr.16:74337347 - 74354133 on Build GRCh38	Loss	LOC283922
dgv853e212	Chr.16:74337368 - 74432521 on Build GRCh38	Gain	LOC105376772 NPIPB15 LOC440386 LOC283922 CLEC18B
nsv833276	Chr.16:74182166 - 74404970 on Build GRCh38	Loss	PSMD7 NPIPB15 LOC440386 LOC283922 LOC101928035
nsv821370	Chr.16:74328208 - 74373921 on Build GRCh38	Duplication	LOC440386 LOC283922
nsv509632	Chr.16:74311644 - 74471617 on Build GRCh38	Insertion	LOC105376772 NPIPB15 LOC440386 LOC283922 GLG1 CLEC18B
esv2758656	Chr.16:74300882 - 74553287 on Build GRCh38	Gain+Loss	LOC105376772 PSMD7 NPIPB15 LOC440386 LOC283922 GLG1 CLEC18B
dgv489n67	Chr.16:74339908 - 74373921 on Build GRCh38	Loss	LOC440386 LOC283922
nsv974833	Chr.16:74325962 - 74373747 on Build GRCh38	Duplication	LOC440386 LOC283922
dgv852e212	Chr.16:74331674 - 74432668 on Build GRCh38	Loss	LOC105376772 NPIPB15 LOC440386 LOC283922 CLEC18B
esv2760420	Chr.16:74316871 - 74422703 on Build GRCh38	Gain+Loss	LOC105376772 NPIPB15 LOC440386 LOC283922 CLEC18B
esv3582311	Chr.16:74332046 - 74373212 on Build GRCh38	Loss	LOC440386 LOC283922
nsv827738	Chr.16:74332140 - 74391805 on Build GRCh38	Gain	NPIPB15 LOC440386 LOC283922
nsv819754	Chr.16:74326479 - 74431235 on Build GRCh38	Loss	LOC105376772 NPIPB15 LOC440386 LOC283922 CLEC18B

More Information

Additional Information:

For this assay, SNP(s) [rs149606595] 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