esv1793437
- 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:211,905
- 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: 1226 SVs from 87 studies. See in: genome view
Overlapping variant regions from other studies: 1226 SVs from 87 studies. See in: genome view
Overlapping variant regions from other studies: 394 SVs from 26 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1793437 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 63,632,006 | 63,843,910 |
| esv1793437 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 64,497,724 | 64,709,628 |
| esv1793437 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 64,180,319 | 64,392,223 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4383081 | Remapped | Perfect | NC_000004.12:g.(?_ 63632006)_(6384391 0_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 63,632,006 | 63,843,910 |
| essv4383081 | Remapped | Perfect | NC_000004.11:g.(?_ 64497724)_(6470962 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 64,497,724 | 64,709,628 |
| essv4383081 | Submitted genomic | NC_000004.10:g.(?_ 64180319)_(6439222 3_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 64,180,319 | 64,392,223 |