Assay Details
Target Gene Details
Entrez Gene ID: | 105369205 |
Gene Name: | uncharacterized LOC105369205 |
Gene Aliases: |
- |
Location: |
Chr.17:20921016-21001059 on Build GRCh38 |
Assay Gene Location: |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC105369205 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1064365 | Chr.17:20898426 - 20987403 on Build GRCh38 | Gain |
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dgv5502n54 | Chr.17:20899465 - 20969018 on Build GRCh38 | Gain |
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esv2751619 | Chr.17:20559595 - 21010843 on Build GRCh38 | Gain |
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nsv1059146 | Chr.17:20849194 - 22546654 on Build GRCh38 | Gain |
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esv3640221 | Chr.17:20913840 - 20955637 on Build GRCh38 | Loss |
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nsv457706 | Chr.17:20911453 - 20969018 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs79483220] 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: |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)