nsv820561
- 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:305,376
- 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: 1761 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1630 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 674 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820561 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 35,221,499 | 35,526,874 |
| nsv820561 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 34,455,870 | 34,761,245 |
| nsv820561 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 34,313,371 | 34,618,746 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421178 | Remapped | Perfect | NC_000016.10:g.(?_ 35221499)_(3552687 4_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,221,499 | 35,526,874 |
| nssv1421178 | Remapped | Perfect | NC_000016.9:g.(?_3 4455870)_(34761245 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 34,455,870 | 34,761,245 |
| nssv1421178 | Submitted genomic | NC_000016.8:g.(?_3 4313371)_(34618746 _?)dup | NCBI36 (hg18) | NC_000016.8 | Chr16 | 34,313,371 | 34,618,746 |