esv2846013
- Organism: Homo sapiens
- Study:estd209 (Pang et al. 2014b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:20,001
- Publication(s):Pang et al. 2014
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: 449 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 286 SVs from 41 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2846013 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | Second Pass | NC_000009.12 | Chr9 | 62,066,156 | 62,086,156 |
| esv2846013 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 67,570,000 | 67,590,000 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7115580 | deletion | HuRef | Sequencing | Read depth | 471,817 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv7115580 | Remapped | Perfect | NC_000009.12:g.(?_ 62066156)_(6208615 6_?)del | GRCh38.p12 | Second Pass | NC_000009.12 | Chr9 | 62,066,156 | 62,086,156 |
| essv7115580 | Submitted genomic | NC_000009.11:g.(?_ 67570000)_(6759000 0_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 67,570,000 | 67,590,000 |