Product Details
- Assay Reference Genome
Location
Chr.15:68211315 on build GRCh38
- Cytoband
- 15q23
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs116956347] 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.
Target Gene Details
- Entrez Gene ID
- 54982
- Gene Symbol
- CLN6
- Gene Name
- ceroid-lipofuscinosis, neuronal 6, late infantile, variant
- Gene Aliases
- CLN4A, HsT18960, nclf
- Location
- Chr.15:68206992-68229742 on build GRCh38
- Assay Gene Location
- Overlaps Intron 4 - Exon 5
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