esv1364928
- 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:14,553
- 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: 569 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 569 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 302 SVs from 24 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1364928 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 1,237,123 | 1,251,675 |
esv1364928 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 1,287,124 | 1,301,676 |
esv1364928 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 1,227,125 | 1,241,677 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv3861808 | Remapped | Perfect | NC_000016.10:g.123 7123_1251675inv | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 1,237,123 | 1,251,675 |
essv3861808 | Remapped | Perfect | NC_000016.9:g.1287 124_1301676inv | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 1,287,124 | 1,301,676 |
essv3861808 | Submitted genomic | NC_000016.8:g.1227 125_1241677inv | NCBI36 (hg18) | NC_000016.8 | Chr16 | 1,227,125 | 1,241,677 |