nsv499308
- Organism: Homo sapiens
- Study:nstd47 (Kidd et al. 2010b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:41,710
- Publication(s):Kidd et al. 2010
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: 779 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 779 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 287 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv499308 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 122,580,319 | 122,622,028 |
| nsv499308 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 124,339,835 | 124,381,544 |
| nsv499308 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 124,329,825 | 124,371,534 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv585633 | copy number loss | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv585633 | Remapped | Perfect | NC_000010.11:g.122 580319_122622028de l | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 122,580,319 | 122,622,028 |
| nssv585633 | Remapped | Perfect | NC_000010.10:g.124 339835_124381544de l | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 124,339,835 | 124,381,544 |
| nssv585633 | Submitted genomic | NC_000010.9:g.1243 29825_124371534del | NCBI36 (hg18) | NC_000010.9 | Chr10 | 124,329,825 | 124,371,534 |