esv4621
- Organism: Homo sapiens
- Study:estd3 (Wang et al. 2008)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:160
- Publication(s):Wang et al. 2008
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: 279 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 279 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 118 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv4621 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 151,313,117 | 151,313,276 |
| esv4621 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 151,010,203 | 151,010,362 |
| esv4621 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 150,641,136 | 150,641,295 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv27062 | inversion | YH | Sequencing | Read depth and paired-end mapping | 2,682 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv27062 | Remapped | Perfect | NC_000007.14:g.(15 1313117_?)_(?_1513 13276)inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 151,313,117 | 151,313,276 |
| essv27062 | Remapped | Perfect | NC_000007.13:g.(15 1010203_?)_(?_1510 10362)inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 151,010,203 | 151,010,362 |
| essv27062 | Submitted genomic | NC_000007.12:g.(15 0641136_?)_(?_1506 41295)inv | NCBI36 (hg18) | NC_000007.12 | Chr7 | 150,641,136 | 150,641,295 |