Assay Details
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: | Overlaps Intron 2 - Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LINC00928 | NR_027074.1 | |||
NR_027075.1 | ||||
NR_027076.1 | ||||
NR_027077.1 |
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 | LOC105371031 LINC00928 RHCG |
nsv1038140 | Chr.15:89141274 - 89620108 on Build GRCh38 | Gain | ABHD2 LOC105370962 MIR6766 MIR9-3HG RLBP1 TICRR MIR9-3 POLG LOC105371031 LINC00928 FANCI RHCG |
nsv1047384 | Chr.15:89498372 - 89571078 on Build GRCh38 | Loss | LOC105371031 LINC00928 |
esv34025 | Chr.15:89412131 - 89630626 on Build GRCh38 | Loss | TICRR KIF7 LOC105371031 LINC00928 RHCG |
More Information
Additional Information:
For this assay, SNP(s) [rs80288912] 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 |