esv3693019
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:299,340
- Publication(s):Palta et al. 2015
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: 1532 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1536 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 538 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3693019 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 12,288,920 | 12,588,259 |
| esv3693019 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 12,288,920 | 12,588,259 |
| esv3693019 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 12,278,920 | 12,578,259 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16509089 | Remapped | Perfect | NC_000009.12:g.(?_ 12288920)_(1258825 9_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,288,920 | 12,588,259 |
| essv16509089 | Remapped | Perfect | NC_000009.11:g.(?_ 12288920)_(1258825 9_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 12,288,920 | 12,588,259 |
| essv16509089 | Submitted genomic | NC_000009.10:g.(?_ 12278920)_(1257825 9_?)del | NCBI36 (hg18) | NC_000009.10 | Chr9 | 12,278,920 | 12,578,259 |