nsv2797775
- Organism: Homo sapiens
- Study:nstd137 (Huddleston et al. 2016)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:674
- Publication(s):Huddleston et al. 2016
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: 212 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 233 SVs from 46 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv2797775 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 43,230,014 | 43,230,687 | ||
| nsv2797775 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 41,382,065 | 41,382,751 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv13702777 | inversion | SAMN03255769 | Sequencing | Local sequence assembly | 46 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv13702777 | Submitted genomic | NC_000017.11:g.432 30014_43230687inv | GRCh38 (hg38) | NC_000017.11 | Chr17 | 43,230,014 | 43,230,687 | ||
| nssv13702777 | Remapped | Good | NC_000017.10:g.413 82065_41382751inv | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 41,382,065 | 41,382,751 |