Genomic Map
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Target Gene Details
Entrez Gene ID: | 102724058 |
Gene Name: | uncharacterized LOC102724058 |
Gene Aliases: |
- |
Location: |
Chr.2:165957418-166036400 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC102724058 | NR_110598.1 | |||
| HY008183.1 | ||||
| HY011842.1 | ||||
| HY029566.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834445 | Chr.2:165800387 - 165995152 on Build GRCh38 | Gain+Loss |
 TTC21B-AS1
LOC100506124
LOC102724058
TTC21B
SCN1A
|
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Additional Information:
For this assay, SNP(s) [rs114130023] 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
|
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