Assay Details
Target Gene Details
Entrez Gene ID: | 1755 |
Gene Name: | deleted in malignant brain tumors 1 |
Gene Aliases: |
GP340, SAG, muclin |
Location: |
Chr.10:122560665-122643736 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv7582 | Chr.10:122575775 - 122587364 on Build GRCh38 | Insertion |
|
| esv2759786 | Chr.10:122503559 - 122695299 on Build GRCh38 | Gain+Loss |
|
| esv2760157 | Chr.10:122574497 - 122591497 on Build GRCh38 | Loss |
|
| nsv1159772 | Chr.10:122548664 - 122597296 on Build GRCh38 | Duplication |
|
| esv3579179 | Chr.10:122575052 - 122597392 on Build GRCh38 | Loss |
|
| nsv508611 | Chr.10:122562819 - 122630985 on Build GRCh38 | Deletion |
|
| nsv552255 | Chr.10:122522412 - 122617922 on Build GRCh38 | Loss |
|
| esv23096 | Chr.10:122546305 - 122617308 on Build GRCh38 | Gain+Loss |
|
| esv3577793 | Chr.10:122574679 - 122598197 on Build GRCh38 | Gain |
|
| nsv1159773 | Chr.10:122564250 - 122629780 on Build GRCh38 | Duplication |
|
| nsv7581 | Chr.10:122569936 - 122639333 on Build GRCh38 | Deletion |
|
More Information
Set Membership: |
|

Genomic Map