nsv482263
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:sequence alteration
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:150,722
- Publication(s):Sharp et al. 2006
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: 399 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 399 SVs from 51 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482263 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 143,856,990 | 144,007,711 |
| nsv482263 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 144,614,559 | 144,765,278 |
| nsv482263 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | GPC_000000200.1 | Chr2 | 144,825,328 | 144,976,047 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3007470 | sequence alteration | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3007470 | Remapped | Good | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 143,856,990 | 144,007,711 |
| nssv3007470 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 144,614,559 | 144,765,278 |
| nssv3007470 | Submitted genomic | NCBI34 (hg16) | GPC_000000200.1 | Chr2 | 144,825,328 | 144,976,047 |