Hs03901414_cn

• Gene Symbol: LOC101927751
• Assay Reference Genome Location: Chr.15:100917447 on build GRCh38
• Cytoband: 15q26.3

Target Gene Details

• Entrez Gene ID: 101927751
• Gene Name: uncharacterized LOC101927751
• Gene Aliases: -
• Location: Chr.15:100892343-100919283 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC101927751	NR_135827.1
	NR_135828.1
	NR_135831.1
	AK126286.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1041172	Chr.15:100435008 - 101062634 on Build GRCh38	Gain	PRKXP1 LOC440313 CERS3 ALDH1A3 ASB7 LOC105369201 LOC101927751 LRRK1 LINS1 CERS3-AS1 LOC102723335
nsv457288	Chr.15:100884530 - 100924371 on Build GRCh38	Loss	ALDH1A3 LOC101927751 LRRK1
nsv469824	Chr.15:100759595 - 100934123 on Build GRCh38	Loss	LOC440313 ALDH1A3 LOC105369201 LOC101927751 LRRK1

More Information

Additional Information:

For this assay, SNP(s) [rs192563054] 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