Assay Details
Target Gene Details
Entrez Gene ID: | 105375975 |
Gene Name: | histone-lysine N-methyltransferase SETMAR-like |
Gene Aliases: |
- |
Location: |
Chr.9:11610222-11618749 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC105375975 | XM_011518088.2 | XP_011516390.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1028493 | Chr.9:11607030 - 11622644 on Build GRCh38 | Gain |
![]() |
esv2422486 | Chr.9:11512989 - 11675590 on Build GRCh38 | Deletion |
![]() |
esv2752276 | Chr.9:11224627 - 11958106 on Build GRCh38 | Loss |
![]() |
esv2761283 | Chr.9:11523636 - 12014548 on Build GRCh38 | Loss |
![]() |
nsv613433 | Chr.9:11606348 - 11716862 on Build GRCh38 | Gain |
![]() |
nsv1017027 | Chr.9:11575785 - 11799681 on Build GRCh38 | Gain |
![]() |
nsv613420 | Chr.9:11200588 - 11619839 on Build GRCh38 | Loss |
![]() |
nsv1018389 | Chr.9:11596157 - 11633767 on Build GRCh38 | Gain |
![]() |
nsv8415 | Chr.9:11173118 - 11631933 on Build GRCh38 | Loss |
![]() |
esv3619616 | Chr.9:11600555 - 11733459 on Build GRCh38 | Loss |
![]() |
esv2752278 | Chr.9:11600500 - 11701727 on Build GRCh38 | Loss |
![]() |
nsv471281 | Chr.9:11453474 - 11716862 on Build GRCh38 | Loss |
![]() |
dgv7412n100 | Chr.9:11582831 - 11934365 on Build GRCh38 | Loss |
![]() |
dgv7411n100 | Chr.9:11459329 - 11631105 on Build GRCh38 | Loss |
![]() |
dgv7413n100 | Chr.9:11600297 - 11841788 on Build GRCh38 | Loss |
![]() |
esv3619615 | Chr.9:11595197 - 11623463 on Build GRCh38 | Loss |
![]() |
esv3619599 | Chr.9:11347309 - 11623122 on Build GRCh38 | Loss |
![]() |
esv3891582 | Chr.9:11511860 - 11787410 on Build GRCh38 | Loss |
![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs78685678] 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: |
![]() ![]() ![]() ![]() |
Panther Classification:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)