Hs03976085_cn

• Gene Symbol: LOC101928205
• Assay Reference Genome Location: Chr.17:72075777 on build GRCh38
• Cytoband: 17q24.3

Target Gene Details

• Entrez Gene ID: 101928205
• Gene Name: uncharacterized LOC101928205
• Gene Aliases: -
• Location: Chr.17:72072333-72093481 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC101928205	NR_110827.1

Target Gene Details

• Entrez Gene ID: 400618
• Gene Name: SOX9 antisense RNA 1
• Gene Aliases: -
• Location: Chr.17:72071042-72120793 on Build GRCh38
• Assay Gene Location: Within Exon 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SOX9-AS1	NR_103738.1	6	1615
	AK056229.1
	AK094963.1	6	1615

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833530	Chr.17:72033949 - 72232973 on Build GRCh38	Gain+Loss	LOC101928205 LOC102723517 SOX9 LINC01152 SOX9-AS1
esv3573809	Chr.17:71977779 - 72157070 on Build GRCh38	Gain	LOC102723505 LOC101928205 LOC102723517 SOX9 LINC01152 SOX9-AS1

More Information

Additional Information:

For this assay, SNP(s) [rs75458938] 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, Intronic, Non-exonic, DGV Variation