Assay Details
Target Gene Details
Entrez Gene ID: | 8100 |
Gene Name: | intraflagellar transport 88 |
Gene Aliases: |
D13S1056E, DAF19, TG737, TTC10, hTg737 |
Location: |
Chr.13:20566446-20691437 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2759925 | Chr.13:20398583 - 20650339 on Build GRCh38 | Loss | IFT88 CRYL1 MIR4499 |
More Information
Additional Information:
For this assay, SNP(s) [rs78505102] 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 |