esv2422430
- Organism: Homo sapiens
- Study:estd196 (Simon-Sanchez et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:95,030
- Publication(s):Simon-Sanchez et al. 2006
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: 860 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 860 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 53 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2422430 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 135,342,736 | 135,437,765 |
| esv2422430 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 138,234,582 | 138,329,611 |
| esv2422430 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000009.9 | Chr9 | 135,460,527 | 135,555,556 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv5161525 | duplication | ND03834 | SNP array | SNP genotyping analysis | essv5161277, essv5161467, essv5161231 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5161525 | Remapped | Perfect | NC_000009.12:g.(?_ 135342736)_(135437 765_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 135,342,736 | 135,437,765 |
| essv5161525 | Remapped | Perfect | NC_000009.11:g.(?_ 138234582)_(138329 611_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 138,234,582 | 138,329,611 |
| essv5161525 | Submitted genomic | NC_000009.9:g.(?_1 35460527)_(1355555 56_?)dup | NCBI35 (hg17) | NC_000009.9 | Chr9 | 135,460,527 | 135,555,556 |