esv2508611
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,465
- Description:originalFile=Yoruban_inv.gff
- Publication(s):McKernan et al. 2009
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: 370 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 370 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 145 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2508611 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 187,495,780 | 187,497,340 | 187,497,582 | 187,498,244 |
| esv2508611 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 187,464,912 | 187,466,472 | 187,466,714 | 187,467,376 |
| esv2508611 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 185,731,535 | 185,733,095 | 185,733,337 | 185,733,999 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5336800 | Remapped | Perfect | NC_000001.11:g.(18 7495780_187497340) _(187497582_187498 244)inv | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 187,495,780 | 187,497,340 | 187,497,582 | 187,498,244 |
| essv5336800 | Remapped | Perfect | NC_000001.10:g.(18 7464912_187466472) _(187466714_187467 376)inv | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 187,464,912 | 187,466,472 | 187,466,714 | 187,467,376 |
| essv5336800 | Submitted genomic | NC_000001.9:g.(185 731535_185733095)_ (185733337_1857339 99)inv | NCBI36 (hg18) | NC_000001.9 | Chr1 | 185,731,535 | 185,733,095 | 185,733,337 | 185,733,999 |