esv1030429
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,134
- Publication(s):Levy et al. 2007
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: 210 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 210 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1030429 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 233,562,717 | 233,577,850 |
esv1030429 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 234,471,364 | 234,486,497 |
esv1030429 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 234,136,102 | 234,151,235 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4259617 | Remapped | Perfect | NC_000002.12:g.233 562717_233577850in v | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 233,562,717 | 233,577,850 |
essv4259617 | Remapped | Perfect | NC_000002.11:g.234 471364_234486497in v | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 234,471,364 | 234,486,497 |
essv4259617 | Submitted genomic | NC_000002.10:g.234 136102_234151235in v | NCBI36 (hg18) | NC_000002.10 | Chr2 | 234,136,102 | 234,151,235 |