nsv818873
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:893
- Publication(s):Wang et al. 2007
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: 320 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 320 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 8 SVs from 2 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818873 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 133,450,180 | 133,451,072 |
| nsv818873 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 133,320,075 | 133,320,967 |
| nsv818873 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 132,825,285 | 132,826,177 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416965 | Remapped | Perfect | NC_000011.10:g.(?_ 133450180)_(133451 072_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 133,450,180 | 133,451,072 |
| nssv1416965 | Remapped | Perfect | NC_000011.9:g.(?_1 33320075)_(1333209 67_?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 133,320,075 | 133,320,967 |
| nssv1416965 | Submitted genomic | NC_000011.8:g.(?_1 32825285)_(1328261 77_?)del | NCBI35 (hg17) | NC_000011.8 | Chr11 | 132,825,285 | 132,826,177 |