nsv827755
- 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:99,577
- 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: 536 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 536 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv827755 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 76,653,229 | 76,752,805 |
| nsv827755 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 76,687,126 | 76,786,702 |
| nsv827755 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 75,244,627 | 75,344,203 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1426307 | Remapped | Perfect | NC_000016.10:g.(?_ 76653229)_(7675280 5_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 76,653,229 | 76,752,805 |
| nssv1426307 | Remapped | Perfect | NC_000016.9:g.(?_7 6687126)_(76786702 _?)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 76,687,126 | 76,786,702 |
| nssv1426307 | Submitted genomic | NC_000016.8:g.(?_7 5244627)_(75344203 _?)del | NCBI36 (hg18) | NC_000016.8 | Chr16 | 75,244,627 | 75,344,203 |