esv24127
- Organism: Homo sapiens
- Study:estd20 (Conrad et al. 2009)
- Variant Type:sequence alteration
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:8,207
- Publication(s):Conrad et al. 2009
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: 244 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 99 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv24127 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 192,270,694 | 192,278,900 |
| esv24127 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 191,988,483 | 191,996,689 |
| esv24127 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 193,471,177 | 193,479,383 |
Variant Call Information
| Variant Call ID | Type | Method |
|---|---|---|
| esv14477 | copy number variation | Merged region |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| esv14477 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 192,270,694 | 192,278,900 |
| esv14477 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 191,988,483 | 191,996,689 |
| esv14477 | Submitted genomic | NCBI36 (hg18) | NC_000003.10 | Chr3 | 193,471,177 | 193,479,383 |