esv2745085
- 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:73,865
- 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: 270 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 268 SVs from 45 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2745085 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 113,080,848 | 113,154,712 |
| esv2745085 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 112,951,570 | 113,025,434 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv6897601 | deletion | SSM099 | Sequencing | Paired-end mapping | 2,492 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv6897601 | Remapped | Perfect | NC_000011.10:g.(11 3080848_?)_(?_1131 54712)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 113,080,848 | 113,154,712 |
| essv6897601 | Submitted genomic | NC_000011.9:g.(112 951570_?)_(?_11302 5434)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 112,951,570 | 113,025,434 |