esv996944
- 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:12,801
- 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: 196 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 196 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 60 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv996944 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 87,924,790 | 87,937,590 |
| esv996944 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 88,845,942 | 88,858,742 |
| esv996944 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 89,064,966 | 89,077,766 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565824 | Remapped | Perfect | NC_000004.12:g.(87 924790_?)_(?_87937 590)inv12801 | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 87,924,790 | 87,937,590 |
| essv3565824 | Remapped | Perfect | NC_000004.11:g.(88 845942_?)_(?_88858 742)inv12801 | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 88,845,942 | 88,858,742 |
| essv3565824 | Submitted genomic | NC_000004.10:g.(89 064966_?)_(?_89077 766)inv12801 | NCBI36 (hg18) | NC_000004.10 | Chr4 | 89,064,966 | 89,077,766 |