nsv820643
- 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:90,341
- 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: 655 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 642 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 151 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820643 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 30,185,378 | 30,275,718 |
| nsv820643 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 29,420,054 | 29,510,394 |
| nsv820643 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 28,033,715 | 28,124,055 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420095 | Remapped | Perfect | NC_000020.11:g.(?_ 30185378)_(3027571 8_?)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 30,185,378 | 30,275,718 |
| nssv1420095 | Remapped | Perfect | NC_000020.10:g.(?_ 29420054)_(2951039 4_?)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 29,420,054 | 29,510,394 |
| nssv1420095 | Submitted genomic | NC_000020.9:g.(?_2 8033715)_(28124055 _?)dup | NCBI36 (hg18) | NC_000020.9 | Chr20 | 28,033,715 | 28,124,055 |