nsv818655
- 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:192,877
- 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: 1209 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1209 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 54 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818655 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 189,381,570 | 189,574,446 |
| nsv818655 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 189,350,700 | 189,543,576 |
| nsv818655 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 186,082,357 | 186,275,233 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417149 | Remapped | Perfect | NC_000001.11:g.(?_ 189381570)_(189574 446_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,381,570 | 189,574,446 |
| nssv1417149 | Remapped | Perfect | NC_000001.10:g.(?_ 189350700)_(189543 576_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,350,700 | 189,543,576 |
| nssv1417149 | Submitted genomic | NC_000001.8:g.(?_1 86082357)_(1862752 33_?)del | NCBI35 (hg17) | NC_000001.8 | Chr1 | 186,082,357 | 186,275,233 |