nsv482379
- 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:194,201
- 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: 792 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 490 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 792 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482379 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 47,625,963 | 47,815,620 |
| nsv482379 | Remapped | Good | GRCh38.p12 | PATCHES | Second Pass | NW_019805496.1 | Chr11|NW_0 19805496.1 | 53,787 | 247,987 |
| nsv482379 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 47,647,515 | 47,837,172 |
| nsv482379 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000011.7 | Chr11 | 47,611,824 | 47,801,481 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3005983 | sequence alteration | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3005983 | Remapped | Good | GRCh38.p12 | Second Pass | NW_019805496.1 | Chr11|NW_0 19805496.1 | 53,787 | 247,987 |
| nssv3005983 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 47,625,963 | 47,815,620 |
| nssv3005983 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 47,647,515 | 47,837,172 |
| nssv3005983 | Submitted genomic | NCBI34 (hg16) | NC_000011.7 | Chr11 | 47,611,824 | 47,801,481 |