esv991034
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:32,059
- Publication(s):Pang et al. 2010
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: 194 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 194 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 63 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv991034 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 8,270,189 | 8,302,247 |
| esv991034 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 8,335,073 | 8,367,131 |
| esv991034 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 8,241,073 | 8,273,131 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564831 | Remapped | Perfect | NC_000019.10:g.(82 70189_?)_(?_830224 7)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 8,270,189 | 8,302,247 |
| essv3564831 | Remapped | Perfect | NC_000019.9:g.(833 5073_?)_(?_8367131 )del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 8,335,073 | 8,367,131 |
| essv3564831 | Submitted genomic | NC_000019.8:g.(824 1073_?)_(?_8273131 )del14675 | NCBI36 (hg18) | NC_000019.8 | Chr19 | 8,241,073 | 8,273,131 |