esv992215
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:20,831
- Publication(s):Pang 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: 990 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 990 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 559 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv992215 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 57,187,336 | 57,208,166 |
| esv992215 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 57,761,470 | 57,782,300 |
| esv992215 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 56,659,471 | 56,680,301 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586043 | Remapped | Perfect | NC_000013.11:g.(?_ 57187336)_(5720816 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 57,187,336 | 57,208,166 |
| essv3586043 | Remapped | Perfect | NC_000013.10:g.(?_ 57761470)_(5778230 0_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 57,761,470 | 57,782,300 |
| essv3586043 | Submitted genomic | NC_000013.9:g.(?_5 6659471)_(56680301 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 56,659,471 | 56,680,301 |