nsv820487
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:135,532
- Publication(s):Ju 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: 559 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 572 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 304 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820487 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 18,413,100 | 18,548,631 |
| nsv820487 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 19,189,577 | 19,325,108 |
| nsv820487 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 18,259,577 | 18,395,108 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421082 | Remapped | Perfect | NC_000014.9:g.(?_1 8413100)_(18548631 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 18,413,100 | 18,548,631 |
| nssv1421082 | Remapped | Perfect | NC_000014.8:g.(?_1 9189577)_(19325108 _?)dup | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 19,189,577 | 19,325,108 |
| nssv1421082 | Submitted genomic | NC_000014.7:g.(?_1 8259577)_(18395108 _?)dup | NCBI36 (hg18) | NC_000014.7 | Chr14 | 18,259,577 | 18,395,108 |