esv2435539
- 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:1,315
- 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: 247 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 247 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 51 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2435539 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 102,422,517 | 102,422,844 | 102,423,760 | 102,423,831 |
| esv2435539 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 103,434,745 | 103,435,072 | 103,435,988 | 103,436,059 |
| esv2435539 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 103,503,921 | 103,504,248 | 103,505,164 | 103,505,235 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5242242 | Remapped | Perfect | NC_000008.11:g.(10 2422517_102422844) _(102423760_102423 831)inv | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 102,422,517 | 102,422,844 | 102,423,760 | 102,423,831 |
| essv5242242 | Remapped | Perfect | NC_000008.10:g.(10 3434745_103435072) _(103435988_103436 059)inv | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 103,434,745 | 103,435,072 | 103,435,988 | 103,436,059 |
| essv5242242 | Submitted genomic | NC_000008.9:g.(103 503921_103504248)_ (103505164_1035052 35)inv | NCBI36 (hg18) | NC_000008.9 | Chr8 | 103,503,921 | 103,504,248 | 103,505,164 | 103,505,235 |