esv2506365
- 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:1,905
- 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: 246 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 247 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 85 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2506365 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 12,391,871 | 12,392,062 | 12,393,584 | 12,393,775 |
| esv2506365 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 12,544,805 | 12,544,996 | 12,546,518 | 12,546,709 |
| esv2506365 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 12,436,072 | 12,436,263 | 12,437,785 | 12,437,976 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5343685 | Remapped | Perfect | NC_000012.12:g.(12 391871_12392062)_( 12393584_12393775) inv | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 12,391,871 | 12,392,062 | 12,393,584 | 12,393,775 |
| essv5343685 | Remapped | Perfect | NC_000012.11:g.(12 544805_12544996)_( 12546518_12546709) inv | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 12,544,805 | 12,544,996 | 12,546,518 | 12,546,709 |
| essv5343685 | Submitted genomic | NC_000012.10:g.(12 436072_12436263)_( 12437785_12437976) inv | NCBI36 (hg18) | NC_000012.10 | Chr12 | 12,436,072 | 12,436,263 | 12,437,785 | 12,437,976 |