Assay Details
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv4n111 | Chr.1:869076 - 914637 on Build GRCh38 | Duplication |
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nsv1004962 | Chr.1:629241 - 915295 on Build GRCh38 | Gain |
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nsv482937 | Chr.1:10001 - 2368561 on Build GRCh38 | Loss |
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nsv950451 | Chr.1:899421 - 1094520 on Build GRCh38 | Deletion |
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nsv509035 | Chr.1:891406 - 985724 on Build GRCh38 | Insertion |
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dgv1n67 | Chr.1:811028 - 914557 on Build GRCh38 | Gain |
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nsv1005935 | Chr.1:805477 - 915295 on Build GRCh38 | Gain |
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esv3584982 | Chr.1:837710 - 917284 on Build GRCh38 | Gain |
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nsv1009537 | Chr.1:841742 - 915295 on Build GRCh38 | Gain |
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nsv428334 | Chr.1:874371 - 1220569 on Build GRCh38 | Gain |
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nsv10161 | Chr.1:776731 - 1777210 on Build GRCh38 | Gain+Loss |
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dgv5n100 | Chr.1:585989 - 1114424 on Build GRCh38 | Gain |
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nsv517709 | Chr.1:817186 - 1275912 on Build GRCh38 | Gain+Loss |
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dgv1n111 | Chr.1:690090 - 939522 on Build GRCh38 | Duplication |
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dgv3n111 | Chr.1:783283 - 939522 on Build GRCh38 | Duplication |
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dgv2n67 | Chr.1:877618 - 1426500 on Build GRCh38 | Gain |
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nsv832980 | Chr.1:848279 - 1007037 on Build GRCh38 | Gain |
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esv3584976 | Chr.1:733250 - 914824 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) [rs114464092] 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)