Hs03118886_cn

• Gene Symbol: LINC00202-1
• Assay Reference Genome Location: Chr.10:26937043 on build GRCh38
• Cytoband: 10p12.1

Target Gene Details

• Entrez Gene ID: 387644
• Gene Name: long intergenic non-protein coding RNA 202-1
• Gene Aliases: C10orf51, LINC00202, NCRNA00202, bB27G4.1
• Location: Chr.10:26931206-26942001 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LINC00202-1	NR_026795.1
	AK097405.1	1	817
	AK128027.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3622706	Chr.10:26935281 - 26939513 on Build GRCh38	Gain	LINC00202-1 ANKRD26
nsv1150190	Chr.10:26935294 - 26939202 on Build GRCh38	Deletion	LINC00202-1 ANKRD26
esv3546053	Chr.10:26935021 - 26939289 on Build GRCh38	Deletion	LINC00202-1 ANKRD26
esv22014	Chr.10:26935743 - 26940649 on Build GRCh38	Gain+Loss	LINC00202-1 ANKRD26
dgv383n106	Chr.10:26935271 - 26939221 on Build GRCh38	Deletion	LINC00202-1 ANKRD26
esv3415799	Chr.10:26640952 - 26944612 on Build GRCh38	Duplication	PDSS1 LINC00202-2 ABI1 LINC00202-1 ANKRD26
esv2750888	Chr.10:26936718 - 26952851 on Build GRCh38	Gain	LINC00202-1 ANKRD26
esv2759740	Chr.10:26872003 - 26941064 on Build GRCh38	Gain+Loss	LINC00202-1 ANKRD26
nsv512154	Chr.10:26933701 - 26938378 on Build GRCh38	Loss	LINC00202-1 ANKRD26
nsv1146165	Chr.10:26935870 - 26940271 on Build GRCh38	Duplication	LINC00202-1 ANKRD26
dgv105e214	Chr.10:26935162 - 26939513 on Build GRCh38	Loss	LINC00202-1 ANKRD26
nsv6154	Chr.10:26923577 - 26937091 on Build GRCh38	Insertion	LINC00202-1
nsv831812	Chr.10:26772577 - 26945338 on Build GRCh38	Gain	ABI1 LINC00202-1 ANKRD26
nsv442174	Chr.10:26936976 - 26939544 on Build GRCh38	Gain+Loss	LINC00202-1 ANKRD26
esv2760143	Chr.10:26936975 - 26939544 on Build GRCh38	Gain+Loss	LINC00202-1 ANKRD26
nsv956331	Chr.10:26935927 - 26940038 on Build GRCh38	Deletion	LINC00202-1 ANKRD26
esv2734473	Chr.10:26935123 - 26939151 on Build GRCh38	Deletion	LINC00202-1 ANKRD26
nsv947784	Chr.10:26935691 - 26946921 on Build GRCh38	Duplication	LINC00202-1 ANKRD26
esv2664616	Chr.10:26927640 - 27310597 on Build GRCh38	Deletion	ACBD5 LRRC37A6P MASTL YME1L1 ARMC4P1 LINC00202-1 ANKRD26
nsv513742	Chr.10:26935749 - 26940300 on Build GRCh38	Insertion	LINC00202-1 ANKRD26
nsv1161934	Chr.10:26934974 - 26941064 on Build GRCh38	Duplication	LINC00202-1 ANKRD26
nsv1036080	Chr.10:26926900 - 26941064 on Build GRCh38	Gain	LINC00202-1 ANKRD26

More Information

Additional Information:

For this assay, SNP(s) [rs74126891] 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