esv3787342
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:506,605
- Description:Chr18:g.25540575_26047179del
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Fujimoto et al. 2012
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: 1209 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 1209 SVs from 69 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3787342 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 27,960,611 | 28,467,215 |
| esv3787342 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 25,540,575 | 26,047,179 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16613996 | deletion | 1737649 | Curated | Curated | 22 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16613996 | Remapped | Perfect | NC_000018.10:g.279 60611_28467215del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 27,960,611 | 28,467,215 |
| essv16613996 | Submitted genomic | NC_000018.9:g.2554 0575_26047179del | GRCh37 (hg19) | NC_000018.9 | Chr18 | 25,540,575 | 26,047,179 |