Assay Details
Target Gene Details
Entrez Gene ID: | 728012 |
Gene Name: | MCHR2 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.6:99994038-100076419 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MCHR2-AS1 | NR_038384.1 | |||
AI635357.1 | ||||
BU154553.1 | ||||
BU853836.1 | ||||
BX097456.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2752086 | Chr.6:99809403 - 100227174 on Build GRCh38 | Gain | MCHR2-AS1 MCHR2 |
dgv6112n100 | Chr.6:99829964 - 100202622 on Build GRCh38 | Gain | MCHR2-AS1 MCHR2 |
nsv428151 | Chr.6:100006066 - 100166527 on Build GRCh38 | Loss | MCHR2-AS1 |
nsv604259 | Chr.6:99855390 - 100194991 on Build GRCh38 | Gain | MCHR2-AS1 MCHR2 |
nsv1024904 | Chr.6:99839200 - 100082800 on Build GRCh38 | Loss | MCHR2-AS1 MCHR2 |
esv3576203 | Chr.6:99830480 - 100195802 on Build GRCh38 | Gain | MCHR2-AS1 MCHR2 |
More Information
Additional Information:
For this assay, SNP(s) [rs115952776,rs77969338] 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 |