Assay Details
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 |