Assay Details
Target Gene Details
Entrez Gene ID: | 101929140 |
Gene Name: | uncharacterized LOC101929140 |
Gene Aliases: |
- |
Location: |
Chr.13:41132928-41236686 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC101929140 | NR_120423.1 | |||
AK056182.1 | ||||
DA634395.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832587 | Chr.13:41030795 - 41224672 on Build GRCh38 | Gain | LOC101929140 WBP4 KBTBD7 KBTBD6 MTRF1 ELF1 MIR3168 |
esv2747299 | Chr.13:41131549 - 41193448 on Build GRCh38 | Deletion | LOC101929140 KBTBD7 KBTBD6 |
More Information
Additional Information:
For this assay, SNP(s) [rs74047676] 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 |