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 Gene Details
Entrez Gene ID: | 339260 |
Gene Name: | uncharacterized LOC339260 |
Gene Aliases: |
- |
Location: |
Chr.17:20938520-20982357 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC339260 | NR_123730.1 | |||
DB066214.1 |
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 | CCDC144NL-AS1 LOC339260 LOC105369205 |
dgv5502n54 | Chr.17:20899465 - 20969018 on Build GRCh38 | Gain | CCDC144NL-AS1 LOC339260 LOC105369205 |
esv2751619 | Chr.17:20559595 - 21010843 on Build GRCh38 | Gain | USP22 CDRT15L2 CCDC144NL-AS1 LOC339260 LOC105369205 MEIS3P2 ABHD17AP6 CCDC144NL LOC100287072 |
nsv1059146 | Chr.17:20849194 - 22546654 on Build GRCh38 | Gain | LINC01563 DHRS7B LOC100996792 FLJ36000 LOC339260 NATD1 UBBP4 KCNJ12 CCDC144NL MAP2K3 USP22 TMEM11 CCDC144NL-AS1 MTRNR2L1 FAM27E5 LOC105369205 C17orf51 KCNJ18 |
esv3640221 | Chr.17:20913840 - 20955637 on Build GRCh38 | Loss | LOC339260 LOC105369205 |
nsv457706 | Chr.17:20911453 - 20969018 on Build GRCh38 | Gain | LOC339260 LOC105369205 |
nsv2006 | Chr.17:20943450 - 20989417 on Build GRCh38 | Deletion | LOC339260 LOC105369205 |
More Information
Additional Information:
For this assay, SNP(s) [rs78880025] 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 |