Hs02812025_cn

• Gene Symbol: LINC01547
• Assay Reference Genome Location: Chr.21:44933300 on build GRCh38
• Cytoband: 21q22.3

Target Gene Details

• Entrez Gene ID: 84536
• Gene Name: long intergenic non-protein coding RNA 1547
• Gene Aliases: C21orf67, C21orf69, PRED54
• Location: Chr.21:44933284-44939913 on Build GRCh38
• Assay Gene Location: Overlaps - Exon 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LINC01547	NR_027128.1
	AY035381.1	2	1109	AAK60445.1
	BM674075.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3647138	Chr.21:44916487 - 44942284 on Build GRCh38	Loss	ITGB2 FAM207A LINC01547 ITGB2-AS1
nsv834110	Chr.21:44896268 - 45085236 on Build GRCh38	Loss	ITGB2 LOC105372836 PICSAR SSR4P1 LINC00163 FAM207A ADARB1 LINC01547 ITGB2-AS1

More Information

Additional Information:

For this assay, SNP(s) [rs73906951] 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, Non-exonic, DGV Variation