Assay Details
Target Gene Details
Entrez Gene ID: | 101928550 |
Gene Name: | SMC2 antisense RNA 1 (head to head) |
Gene Aliases: |
- |
Location: |
Chr.9:104080024-104092474 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SMC2-AS1 | NR_121580.1 | |||
AK125887.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv7695n100 | Chr.9:104042528 - 104090136 on Build GRCh38 | Loss | SMC2-AS1 |
esv2761294 | Chr.9:104048899 - 104090136 on Build GRCh38 | Loss | SMC2-AS1 |
nsv831676 | Chr.9:103901194 - 104112176 on Build GRCh38 | Gain | SMC2 SMC2-AS1 LOC101928523 |
nsv615049 | Chr.9:103527145 - 104134528 on Build GRCh38 | Gain | SMC2 SMC2-AS1 LOC101928523 |
nsv1045887 | Chr.9:104059467 - 104090136 on Build GRCh38 | Loss | SMC2-AS1 |
nsv615064 | Chr.9:103811066 - 104367820 on Build GRCh38 | Gain | SMC2 LOC105376194 LOC107987034 SMC2-AS1 LOC101928523 |
More Information
Additional Information:
For this assay, SNP(s) [rs78633445] 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 |