esv3692
- 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:330
- 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: 129 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 129 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 46 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 |
---|---|---|---|---|---|---|---|---|---|
esv3692 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 36,309,647 | 36,309,976 |
esv3692 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 36,331,197 | 36,331,526 |
esv3692 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 36,287,773 | 36,288,102 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv26133 | 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 |
---|---|---|---|---|---|---|---|---|---|
essv26133 | Remapped | Perfect | NC_000011.10:g.(36 309647_?)_(?_36309 976)inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 36,309,647 | 36,309,976 |
essv26133 | Remapped | Perfect | NC_000011.9:g.(363 31197_?)_(?_363315 26)inv | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 36,331,197 | 36,331,526 |
essv26133 | Submitted genomic | NC_000011.8:g.(362 87773_?)_(?_362881 02)inv | NCBI36 (hg18) | NC_000011.8 | Chr11 | 36,287,773 | 36,288,102 |