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: | Overlaps Intron 41 - Exon 42 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2759786 | Chr.10:122503559 - 122695299 on Build GRCh38 | Gain+Loss |
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esv2676690 | Chr.10:122610194 - 122618347 on Build GRCh38 | Deletion |
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nsv1159773 | Chr.10:122564250 - 122629780 on Build GRCh38 | Duplication |
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nsv7583 | Chr.10:122592545 - 122619520 on Build GRCh38 | Insertion |
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nsv499097 | Chr.10:122603268 - 122619008 on Build GRCh38 | Loss |
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esv3624776 | Chr.10:122580099 - 122618150 on Build GRCh38 | Loss |
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nsv56 | Chr.10:122598443 - 122627790 on Build GRCh38 | Deletion |
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nsv8731 | Chr.10:122579399 - 122622194 on Build GRCh38 | Gain+Loss |
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esv3624782 | Chr.10:122602807 - 122624657 on Build GRCh38 | Gain |
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esv3546970 | Chr.10:122592440 - 122623563 on Build GRCh38 | Deletion |
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nsv508611 | Chr.10:122562819 - 122630985 on Build GRCh38 | Deletion |
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nsv948210 | Chr.10:122592000 - 122619400 on Build GRCh38 | Duplication |
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dgv294e212 | Chr.10:122582087 - 122622928 on Build GRCh38 | Loss |
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esv1000689 | Chr.10:122600747 - 122618040 on Build GRCh38 | Deletion |
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dgv299e212 | Chr.10:122598537 - 122622928 on Build GRCh38 | Loss |
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nsv499308 | Chr.10:122580319 - 122622028 on Build GRCh38 | Loss |
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nsv951866 | Chr.10:122600785 - 122618884 on Build GRCh38 | Deletion |
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nsv819547 | Chr.10:122579409 - 122619326 on Build GRCh38 | Gain |
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nsv7581 | Chr.10:122569936 - 122639333 on Build GRCh38 | Deletion |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Set Membership: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)