nsv826063
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:99,012
- Publication(s):Park 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: 465 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 465 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 147 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv826063 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 103,154,314 | 103,253,325 |
| nsv826063 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 103,025,043 | 103,124,054 |
| nsv826063 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 102,530,253 | 102,629,264 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1441361 | Remapped | Perfect | NC_000011.10:g.(?_ 103154314)_(103253 325_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 103,154,314 | 103,253,325 |
| nssv1441361 | Remapped | Perfect | NC_000011.9:g.(?_1 03025043)_(1031240 54_?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 103,025,043 | 103,124,054 |
| nssv1441361 | Submitted genomic | NC_000011.8:g.(?_1 02530253)_(1026292 64_?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 102,530,253 | 102,629,264 |