nsv433418
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:77,627
- Publication(s):Cooper 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: 751 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 776 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 17 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433418 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 50,344,953 | 50,422,579 |
| nsv433418 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 50,304,124 | 50,381,750 |
| nsv433418 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 50,260,700 | 50,338,326 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463299 | Remapped | Perfect | NC_000011.10:g.(?_ 50344953)_(5042257 9_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,344,953 | 50,422,579 |
| nssv463299 | Remapped | Perfect | NC_000011.9:g.(?_5 0304124)_(50381750 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 50,304,124 | 50,381,750 |
| nssv463299 | Submitted genomic | NC_000011.8:g.(?_5 0260700)_(50338326 _?)dup | NCBI35 (hg17) | NC_000011.8 | Chr11 | 50,260,700 | 50,338,326 |