nsv821188
- 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:59,461
- 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: 406 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 412 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 104 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821188 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 207,522,388 | 207,581,848 |
| nsv821188 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 207,695,733 | 207,755,193 |
| nsv821188 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 205,762,356 | 205,821,816 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420924 | Remapped | Perfect | NC_000001.11:g.(?_ 207522388)_(207581 848_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 207,522,388 | 207,581,848 |
| nssv1420924 | Remapped | Perfect | NC_000001.10:g.(?_ 207695733)_(207755 193_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 207,695,733 | 207,755,193 |
| nssv1420924 | Submitted genomic | NC_000001.9:g.(?_2 05762356)_(2058218 16_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 205,762,356 | 205,821,816 |