nsv1067819
- Organism: Homo sapiens
- Study:nstd98 (Campbell et al. 2014b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,376,008
- Publication(s):Campbell et al. 2014
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: 7653 SVs from 113 studies. See in: genome view
Overlapping variant regions from other studies: 7653 SVs from 113 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067819 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 112,420,522 | 112,420,588 | 115,796,463 | 115,796,529 |
| nsv1067819 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 112,139,369 | 112,139,435 | 115,515,310 | 115,515,376 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761538 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761538 | Remapped | Perfect | NC_000003.12:g.(11 2420522_112420588) _(115796463_115796 529)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 112,420,522 | 112,420,588 | 115,796,463 | 115,796,529 |
| nssv3761538 | Submitted genomic | NC_000003.11:g.(11 2139369_112139435) _(115515310_115515 376)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 112,139,369 | 112,139,435 | 115,515,310 | 115,515,376 |