Assay Details
Target Gene Details
Entrez Gene ID: | 285194 |
Gene Name: | tumor suppressor candidate 7 (non-protein coding) |
Gene Aliases: |
LINC00902, LSAMP-AS1, LSAMP-AS3, LSAMPAS3, NCRNA00295 |
Location: |
Chr.3:116709788-116717040 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TUSC7 | NR_015391.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv829686 | Chr.3:116606775 - 116775694 on Build GRCh38 | Gain |
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esv3893770 | Chr.3:116409243 - 116721198 on Build GRCh38 | Gain |
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dgv295n21 | Chr.3:116676731 - 116866434 on Build GRCh38 | Loss |
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nsv1011135 | Chr.3:116380194 - 119036472 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs72949409] 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: |
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