nsv5311699
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:372,355
- Publication(s):Chen et al. 2021
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1564 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1564 SVs from 79 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5311699 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000003.12 | Chr3 | 9,776,425 (-298, +9) | 10,148,779 (-10, +290) | ||
| nsv5311699 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 9,818,109 (-298, +9) | 10,190,463 (-10, +290) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16748875 | duplication | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16748875 | Submitted genomic | NC_000003.12:g.(97 76127_9776434)_(10 148769_10149069)du p | GRCh38.p13 | NC_000003.12 | Chr3 | 9,776,425 (-298, +9) | 10,148,779 (-10, +290) | ||
| nssv16748875 | Remapped | Perfect | NC_000003.11:g.(98 17811_9818118)_(10 190453_10190753)du p | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 9,818,109 (-298, +9) | 10,190,463 (-10, +290) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
| Variant Call ID | Allele Frequency (AF) |
|---|---|
| nssv16748875 | <0.001 |