nsv1067812
- 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:3,376,000
- 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: 7652 SVs from 113 studies. See in: genome view
Overlapping variant regions from other studies: 7652 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067812 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 112,420,706 | 112,420,764 | 115,796,647 | 115,796,705 |
| nsv1067812 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 112,139,553 | 112,139,611 | 115,515,494 | 115,515,552 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761532 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761532 | Remapped | Perfect | NC_000003.12:g.(11 2420706_112420764) _(115796647_115796 705)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 112,420,706 | 112,420,764 | 115,796,647 | 115,796,705 |
| nssv3761532 | Submitted genomic | NC_000003.11:g.(11 2139553_112139611) _(115515494_115515 552)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 112,139,553 | 112,139,611 | 115,515,494 | 115,515,552 |