nsv1619
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:33,755
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 213 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 213 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 7 SVs from 3 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1619 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 76,312,275 | 76,346,029 |
| nsv1619 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 76,604,616 | 76,638,370 |
| nsv1619 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 74,391,671 | 74,425,425 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv7200 | Remapped | Perfect | NC_000015.10:g.(76 312275_?)_(?_76346 029)ins5686 | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 76,312,275 | 76,346,029 |
| nssv7200 | Remapped | Perfect | NC_000015.9:g.(766 04616_?)_(?_766383 70)ins5686 | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 76,604,616 | 76,638,370 |
| nssv7200 | Submitted genomic | NC_000015.8:g.(743 91671_?)_(?_744254 25)ins5686 | NCBI35 (hg17) | NC_000015.8 | Chr15 | 74,391,671 | 74,425,425 |