Hs03865033_cn

• Gene Symbol: SOX21-AS1
• Assay Reference Genome Location: Chr.13:94712823 on build GRCh38
• Cytoband: 13q32.1

Target Gene Details

• Entrez Gene ID: 100507533
• Gene Name: SOX21 antisense RNA 1 (head to head)
• Gene Aliases: -
• Location: Chr.13:94712716-94715945 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SOX21-AS1	NR_046514.1	1	108
	AK055459.1	1	110

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1070605	Chr.13:94711245 - 94714046 on Build GRCh38	Deletion	SOX21 SOX21-AS1
nsv832686	Chr.13:94554488 - 94748738 on Build GRCh38	Gain	TGDS SOX21 SOX21-AS1 LOC101927248 GPR180
esv28079	Chr.13:94710850 - 94713584 on Build GRCh38	Loss	SOX21 SOX21-AS1
esv34004	Chr.13:94254283 - 94740390 on Build GRCh38	Loss	GPC6 DCT TGDS SOX21 SOX21-AS1 LOC101927248 GPR180
nsv562766	Chr.13:94712121 - 94713517 on Build GRCh38	Loss	SOX21 SOX21-AS1
nsv826750	Chr.13:94706248 - 94715816 on Build GRCh38	Gain	SOX21 SOX21-AS1 LOC101927248
dgv3326n54	Chr.13:94711363 - 94713465 on Build GRCh38	Loss	SOX21 SOX21-AS1

More Information

Additional Information:

For this assay, SNP(s) [rs536137591] 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, Exonic, DGV Variation