nsv428332
- 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:97,351
- 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: 1086 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 455 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 1069 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 318 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428332 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 493,387 | 590,737 |
| nsv428332 | Remapped | Perfect | GRCh38.p12 | PATCHES | Second Pass | NW_017363817.1 | Chr17|NW_0 17363817.1 | 52,864 | 150,214 |
| nsv428332 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 396,627 | 493,977 |
| nsv428332 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 343,377 | 440,727 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv453296 | Remapped | Perfect | NW_017363817.1:g.( ?_52864)_(150214_? )del | GRCh38.p12 | Second Pass | NW_017363817.1 | Chr17|NW_0 17363817.1 | 52,864 | 150,214 |
| nssv453296 | Remapped | Perfect | NC_000017.11:g.(?_ 493387)_(590737_?) del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 493,387 | 590,737 |
| nssv453296 | Remapped | Perfect | NC_000017.10:g.(?_ 396627)_(493977_?) del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 396,627 | 493,977 |
| nssv453296 | Submitted genomic | NC_000017.9:g.(?_3 43377)_(440727_?)d el | NCBI36 (hg18) | NC_000017.9 | Chr17 | 343,377 | 440,727 |