esv1003190
- 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:21,911
- 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: 163 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 163 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 32 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1003190 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 38,511,317 | 38,533,227 |
| esv1003190 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000022.10 | Chr22 | 38,907,322 | 38,929,232 |
| esv1003190 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000022.9 | Chr22 | 37,237,268 | 37,259,178 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564922 | Remapped | Perfect | NC_000022.11:g.(38 511317_?)_(?_38533 227)inv21911 | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 38,511,317 | 38,533,227 |
| essv3564922 | Remapped | Perfect | NC_000022.10:g.(38 907322_?)_(?_38929 232)inv21911 | GRCh37.p13 | First Pass | NC_000022.10 | Chr22 | 38,907,322 | 38,929,232 |
| essv3564922 | Submitted genomic | NC_000022.9:g.(372 37268_?)_(?_372591 78)inv21911 | NCBI36 (hg18) | NC_000022.9 | Chr22 | 37,237,268 | 37,259,178 |