Assay Details
Target Gene Details
Entrez Gene ID: | 6929 |
Gene Name: | transcription factor 3 |
Gene Aliases: |
AGM8, E2A, E47, ITF1, TCF-3, VDIR, bHLHb21 |
Location: |
Chr.19:1609290-1652590 on Build GRCh38 |
Assay Gene Location: | Within Exon 20 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv32942 | Chr.19:1320268 - 1999205 on Build GRCh38 | Gain+Loss |
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nsv953942 | Chr.19:1371602 - 2057401 on Build GRCh38 | Deletion |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs113708250] 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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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)