esv1849899
- 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:418,628
- 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: 1686 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1686 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 520 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1849899 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 15,054,114 | 15,472,741 |
| esv1849899 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 14,911,623 | 15,330,250 |
| esv1849899 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 14,955,994 | 15,374,621 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4403054 | Remapped | Perfect | NC_000008.11:g.(?_ 15054114)_(1547274 1_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 15,054,114 | 15,472,741 |
| essv4403054 | Remapped | Perfect | NC_000008.10:g.(?_ 14911623)_(1533025 0_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 14,911,623 | 15,330,250 |
| essv4403054 | Submitted genomic | NC_000008.9:g.(?_1 4955994)_(15374621 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 14,955,994 | 15,374,621 |