Genomic Map
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Target Gene Details
Entrez Gene ID: | 102724691 |
Gene Name: | uncharacterized LOC102724691 |
Gene Aliases: |
- |
Location: |
Chr.2:104936241-105038496 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC102724691 | NR_110603.1 | |||
| BX109606.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv961846 | Chr.2:104977941 - 104980336 on Build GRCh38 | Duplication |
 LOC102724691
|
| nsv2862 | Chr.2:104945544 - 104980488 on Build GRCh38 | Insertion |
LOC102724691
|
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Additional Information:
For this assay, SNP(s) [rs192625366] 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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