esv2738343
- Organism: Homo sapiens
- Study:estd201 (Wong et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:47,181
- Publication(s):Wong et al. 2013
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: 374 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 380 SVs from 46 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2738343 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 28,908,275 | 28,955,455 |
| esv2738343 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 28,908,273 | 28,955,453 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv6724001 | deletion | SSM045 | Sequencing | Paired-end mapping | 3,460 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv6724001 | Remapped | Perfect | NC_000009.12:g.(28 908275_?)_(?_28955 455)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 28,908,275 | 28,955,455 |
| essv6724001 | Submitted genomic | NC_000009.11:g.(28 908273_?)_(?_28955 453)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 28,908,273 | 28,955,453 |