esv1850449
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:141,964
- Publication(s):Pinto et al. 2011
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: 2707 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 2710 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 1759 SVs from 28 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1850449 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 32,581,418 | 32,723,381 |
| esv1850449 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 32,592,739 | 32,734,702 |
| esv1850449 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 32,500,240 | 32,642,203 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4414778 | Remapped | Perfect | NC_000016.10:g.(?_ 32581418)_(3272338 1_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,581,418 | 32,723,381 |
| essv4414778 | Remapped | Perfect | NC_000016.9:g.(?_3 2592739)_(32734702 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 32,592,739 | 32,734,702 |
| essv4414778 | Submitted genomic | NC_000016.8:g.(?_3 2500240)_(32642203 _?)dup | NCBI36 (hg18) | NC_000016.8 | Chr16 | 32,500,240 | 32,642,203 |