nsv818130
- 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:88,331
- 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: 382 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 382 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 28 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818130 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 21,215,817 | 21,304,147 |
| nsv818130 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 21,257,309 | 21,345,639 |
| nsv818130 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000003.9 | Chr3 | 21,232,313 | 21,320,643 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418050 | Remapped | Perfect | NC_000003.12:g.(?_ 21215817)_(2130414 7_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 21,215,817 | 21,304,147 |
| nssv1418050 | Remapped | Perfect | NC_000003.11:g.(?_ 21257309)_(2134563 9_?)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 21,257,309 | 21,345,639 |
| nssv1418050 | Submitted genomic | NC_000003.9:g.(?_2 1232313)_(21320643 _?)dup | NCBI35 (hg17) | NC_000003.9 | Chr3 | 21,232,313 | 21,320,643 |