esv2489937
- 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:5,244
- 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: 423 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 319 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2489937 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 62,813,331 | 62,813,381 | 62,818,154 | 62,818,574 |
| esv2489937 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 66,469,155 | 66,469,205 | 66,473,978 | 66,474,398 |
| esv2489937 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 66,208,975 | 66,209,025 | 66,213,798 | 66,214,218 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5249900 | Remapped | Perfect | NC_000009.12:g.(62 813331_62813381)_( 62818154_62818574) inv | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 62,813,331 | 62,813,381 | 62,818,154 | 62,818,574 |
| essv5249900 | Remapped | Perfect | NC_000009.11:g.(66 469155_66469205)_( 66473978_66474398) inv | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 66,469,155 | 66,469,205 | 66,473,978 | 66,474,398 |
| essv5249900 | Submitted genomic | NC_000009.10:g.(66 208975_66209025)_( 66213798_66214218) inv | NCBI36 (hg18) | NC_000009.10 | Chr9 | 66,208,975 | 66,209,025 | 66,213,798 | 66,214,218 |