esv5324
- 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:6,029
- 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: 182 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 182 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 57 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 | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv5324 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 55,007,403 | 55,013,431 |
| esv5324 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 56,767,163 | 56,773,191 |
| esv5324 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 56,437,169 | 56,443,197 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv27765 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| essv27765 | Remapped | Perfect | NC_000010.11:g.(55 007403_?)_(?_55013 431)inv | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 55,007,403 | 55,013,431 |
| essv27765 | Remapped | Perfect | NC_000010.10:g.(56 767163_?)_(?_56773 191)inv | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 56,767,163 | 56,773,191 |
| essv27765 | Submitted genomic | NC_000010.9:g.(564 37169_?)_(?_564431 97)inv | NCBI36 (hg18) | NC_000010.9 | Chr10 | 56,437,169 | 56,443,197 |