nsv433208
- 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:73,002
- 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: 318 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 318 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 12 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433208 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 154,088,191 | 154,161,192 |
| nsv433208 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 154,944,704 | 155,017,705 |
| nsv433208 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000002.9 | Chr2 | 154,770,212 | 154,843,213 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463089 | Remapped | Perfect | NC_000002.12:g.(?_ 154088191)_(154161 192_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 154,088,191 | 154,161,192 |
| nssv463089 | Remapped | Perfect | NC_000002.11:g.(?_ 154944704)_(155017 705_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 154,944,704 | 155,017,705 |
| nssv463089 | Submitted genomic | NC_000002.9:g.(?_1 54770212)_(1548432 13_?)del | NCBI35 (hg17) | NC_000002.9 | Chr2 | 154,770,212 | 154,843,213 |