esv989801
- 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:20,677
- 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: 184 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 184 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv989801 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 57,374,252 | 57,394,928 |
| esv989801 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 57,768,035 | 57,788,711 |
| esv989801 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 56,054,302 | 56,074,978 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564367 | Remapped | Perfect | NC_000012.12:g.(57 374252_?)_(?_57394 928)inv20677 | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 57,374,252 | 57,394,928 |
| essv3564367 | Remapped | Perfect | NC_000012.11:g.(57 768035_?)_(?_57788 711)inv20677 | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 57,768,035 | 57,788,711 |
| essv3564367 | Submitted genomic | NC_000012.10:g.(56 054302_?)_(?_56074 978)inv20677 | NCBI36 (hg18) | NC_000012.10 | Chr12 | 56,054,302 | 56,074,978 |