nsv821057
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,816
- Publication(s):Ju et al. 2010
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: 897 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 897 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821057 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 101,751,531 | 101,765,346 |
| nsv821057 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 102,291,734 | 102,305,549 |
| nsv821057 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 100,109,257 | 100,123,072 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421150 | Remapped | Perfect | NC_000015.10:g.(?_ 101751531)_(101765 346_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 101,751,531 | 101,765,346 |
| nssv1421150 | Remapped | Perfect | NC_000015.9:g.(?_1 02291734)_(1023055 49_?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 102,291,734 | 102,305,549 |
| nssv1421150 | Submitted genomic | NC_000015.8:g.(?_1 00109257)_(1001230 72_?)del | NCBI36 (hg18) | NC_000015.8 | Chr15 | 100,109,257 | 100,123,072 |