nsv433350
- 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:20,742
- 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: 273 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 278 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 13 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433350 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 225,477,582 | 225,498,323 |
| nsv433350 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 225,665,284 | 225,686,025 |
| nsv433350 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 221,972,019 | 221,992,760 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463231 | Remapped | Perfect | NC_000001.11:g.(?_ 225477582)_(225498 323_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 225,477,582 | 225,498,323 |
| nssv463231 | Remapped | Perfect | NC_000001.10:g.(?_ 225665284)_(225686 025_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 225,665,284 | 225,686,025 |
| nssv463231 | Submitted genomic | NC_000001.8:g.(?_2 21972019)_(2219927 60_?)dup | NCBI35 (hg17) | NC_000001.8 | Chr1 | 221,972,019 | 221,992,760 |