nsv428125
- 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:263,599
- 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: 980 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 980 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 282 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428125 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 120,859,173 | 121,122,771 |
| nsv428125 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 120,194,868 | 120,458,466 |
| nsv428125 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 120,222,767 | 120,486,365 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv450495 | Remapped | Perfect | NC_000005.10:g.(?_ 120859173)_(121122 771_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 120,859,173 | 121,122,771 |
| nssv450495 | Remapped | Perfect | NC_000005.9:g.(?_1 20194868)_(1204584 66_?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 120,194,868 | 120,458,466 |
| nssv450495 | Submitted genomic | NC_000005.8:g.(?_1 20222767)_(1204863 65_?)dup | NCBI36 (hg18) | NC_000005.8 | Chr5 | 120,222,767 | 120,486,365 |