nsv825278
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:85,959
- Publication(s):Park 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: 322 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 322 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 110 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv825278 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 20,152,077 | 20,238,035 |
| nsv825278 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 20,441,006 | 20,526,964 |
| nsv825278 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 20,481,012 | 20,566,970 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1439042 | Remapped | Perfect | NC_000010.11:g.(?_ 20152077)_(2023803 5_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 20,152,077 | 20,238,035 |
| nssv1439042 | Remapped | Perfect | NC_000010.10:g.(?_ 20441006)_(2052696 4_?)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 20,441,006 | 20,526,964 |
| nssv1439042 | Submitted genomic | NC_000010.9:g.(?_2 0481012)_(20566970 _?)del | NCBI36 (hg18) | NC_000010.9 | Chr10 | 20,481,012 | 20,566,970 |