Hs05343947_cn

• Gene Symbol: LINC00928
• Assay Reference Genome Location: Chr.15:89516716 on build GRCh38
• Cytoband: 15q26.1

Target Gene Details

• Entrez Gene ID: 283761
• Gene Name: long intergenic non-protein coding RNA 928
• Gene Aliases: -
• Location: Chr.15:89504930-89524034 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LINC00928	NR_027074.1
	NR_027075.1
	NR_027076.1
	NR_027077.1
	AK058110.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv570386	Chr.15:89464359 - 89517327 on Build GRCh38	Loss	RHCG LINC00928 LOC105371031
nsv1038140	Chr.15:89141274 - 89620108 on Build GRCh38	Gain	ABHD2 RLBP1 TICRR RHCG LINC00928 MIR9-3 MIR9-3HG POLG LOC105371031 MIR6766 FANCI LOC105370962
esv3637197	Chr.15:89515971 - 89518616 on Build GRCh38	Loss	LINC00928
nsv1047384	Chr.15:89498372 - 89571078 on Build GRCh38	Loss	LINC00928 LOC105371031
esv34025	Chr.15:89412131 - 89630626 on Build GRCh38	Loss	TICRR RHCG LINC00928 KIF7 LOC105371031
esv3552827	Chr.15:89516126 - 89518554 on Build GRCh38	Deletion	LINC00928
esv2663545	Chr.15:89516027 - 89518584 on Build GRCh38	Deletion	LINC00928

More Information

Additional Information:

For this assay, SNP(s) [rs113146805] 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