esv1001323
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,319
- 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: 253 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 253 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 146 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1001323 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 85,584,958 | 85,604,276 |
| esv1001323 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 85,618,564 | 85,637,882 |
| esv1001323 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 84,176,065 | 84,195,383 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564450 | Remapped | Perfect | NC_000016.10:g.(85 584958_?)_(?_85604 276)inv19319 | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 85,584,958 | 85,604,276 |
| essv3564450 | Remapped | Perfect | NC_000016.9:g.(856 18564_?)_(?_856378 82)inv19319 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 85,618,564 | 85,637,882 |
| essv3564450 | Submitted genomic | NC_000016.8:g.(841 76065_?)_(?_841953 83)inv19319 | NCBI36 (hg18) | NC_000016.8 | Chr16 | 84,176,065 | 84,195,383 |