nsv428419
- Organism: Homo sapiens
- Study:nstd8 (Perry et al. 2008b)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:205,469
- Publication(s):Perry et al. 2008
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: 421 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 421 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 85 SVs from 16 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv428419 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 97,497,948 | 97,703,416 |
| nsv428419 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 97,216,792 | 97,422,260 |
| nsv428419 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 98,699,482 | 98,904,950 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv454272 | Remapped | Perfect | NC_000003.12:g.(?_ 97497948)_(9770341 6_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 97,497,948 | 97,703,416 |
| nssv454272 | Remapped | Perfect | NC_000003.11:g.(?_ 97216792)_(9742226 0_?)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 97,216,792 | 97,422,260 |
| nssv454272 | Submitted genomic | NC_000003.10:g.(?_ 98699482)_(9890495 0_?)dup | NCBI36 (hg18) | NC_000003.10 | Chr3 | 98,699,482 | 98,904,950 |