esv993745
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,304
- Publication(s):Pang et al. 2010
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: 128 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 35 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv993745 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 99,004,779 | 99,022,082 |
| esv993745 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 99,621,242 | 99,638,545 |
| esv993745 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 98,987,674 | 99,004,977 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564235 | Remapped | Perfect | NC_000002.12:g.(99 004779_?)_(?_99022 082)inv17304 | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 99,004,779 | 99,022,082 |
| essv3564235 | Remapped | Perfect | NC_000002.11:g.(99 621242_?)_(?_99638 545)inv17304 | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 99,621,242 | 99,638,545 |
| essv3564235 | Submitted genomic | NC_000002.10:g.(98 987674_?)_(?_99004 977)inv17304 | NCBI36 (hg18) | NC_000002.10 | Chr2 | 98,987,674 | 99,004,977 |