Hs03352325_cn

• Gene Symbol: SLC16A1-AS1
• Assay Reference Genome Location: Chr.1:112957830 on build GRCh38
• Cytoband: 1p13.2

Target Gene Details

• Entrez Gene ID: 100506392
• Gene Name: SLC16A1 antisense RNA 1
• Gene Aliases: -
• Location: Chr.1:112956415-112964072 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC16A1-AS1	NR_103743.1
	NR_103744.1
	BQ708590.1
	BX648855.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3584026	Chr.1:112761723 - 113036481 on Build GRCh38	Gain	AKR7A2P1 SLC16A1-AS1 SLC16A1 LOC100996251 LINC01356 HP08777
nsv1004102	Chr.1:112753183 - 113008588 on Build GRCh38	Gain	AKR7A2P1 SLC16A1-AS1 SLC16A1 LINC01356 HP08777
esv24626	Chr.1:112832815 - 113310193 on Build GRCh38	Loss	AKR7A2P1 SLC16A1-AS1 LOC102723919 SLC16A1 LOC100996251 LOC643441 LRIG2 LINC01356 HP08777
nsv999915	Chr.1:112817523 - 113142211 on Build GRCh38	Gain	AKR7A2P1 SLC16A1-AS1 LOC102723919 SLC16A1 LOC100996251 LRIG2 LINC01356 HP08777
esv3894045	Chr.1:112927499 - 113179081 on Build GRCh38	Gain	SLC16A1-AS1 LOC102723919 SLC16A1 LOC100996251 LRIG2

More Information

Additional Information:

For this assay, SNP(s) [rs75737835] 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