Hs03449093_cn

• Gene Symbol: LOC339874
• Assay Reference Genome Location: Chr.3:131376672 on build GRCh38
• Cytoband: 3q22.1

Target Gene Details

• Entrez Gene ID: 339874
• Gene Name: uncharacterized LOC339874
• Gene Aliases: -
• Location: Chr.3:131325092-131381475 on Build GRCh38
• Assay Gene Location: Overlaps Intron 1 - Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC339874	NR_038976.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3597785	Chr.3:131350870 - 131415049 on Build GRCh38	Gain	NUDT16 LOC339874 NUDT16P1
esv3597781	Chr.3:131272356 - 131472358 on Build GRCh38	Gain	NUDT16 NEK11 LOC339874 MRPL3 NUDT16P1
nsv829724	Chr.3:131366925 - 131557541 on Build GRCh38	Gain	BCL2L12P1 NUDT16 CPNE4 LOC339874 MRPL3 SNORA58
dgv934e214	Chr.3:131361494 - 131382962 on Build GRCh38	Loss	NUDT16 LOC339874 NUDT16P1

More Information

Additional Information:

For this assay, SNP(s) [rs118184987,rs151315684] 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, Non-exonic, DGV Variation