Hs06659375_cn

• Gene Symbol: ALDH1L1-AS2
• Assay Reference Genome Location: Chr.3:126206732 on build GRCh38
• Cytoband: 3q21.3

Target Gene Details

• Entrez Gene ID: 100862662
• Gene Name: ALDH1L1 antisense RNA 2
• Gene Aliases: -
• Location: Chr.3:126180065-126210169 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ALDH1L1-AS2	NR_046383.1
	DA256650.1
	DA566603.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3597677	Chr.3:126206612 - 126209251 on Build GRCh38	Loss	ALDH1L1-AS2
nsv3985	Chr.3:126173880 - 126218546 on Build GRCh38	Deletion	ALDH1L1-AS2 ALDH1L1
dgv8545n54	Chr.3:126091128 - 126251891 on Build GRCh38	Loss	ALDH1L1-AS2 SLC41A3 ALDH1L1-AS1 ALDH1L1
nsv1007256	Chr.3:126163635 - 126238737 on Build GRCh38	Gain	ALDH1L1-AS2 ALDH1L1

More Information

Additional Information:

For this assay, SNP(s) [rs76514835] 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