nsv3168001
- Organism: Homo sapiens
- Study:nstd158 (Cleal et al. 2019)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:94,755
- Publication(s):Cleal et al. 2019
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: 221 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 214 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3168001 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 14,756,316 (-2, +2) | 14,851,070 (-2, +2) |
| nsv3168001 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 14,777,862 (-2, +2) | 14,872,616 (-2, +2) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14240004 | inversion | DB81 | Sequencing | Paired-end mapping | 14 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14240004 | Remapped | Perfect | NC_000011.10:g.(14 756314_14756318)_( 14851068_14851072) inv174 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 14,756,316 (-2, +2) | 14,851,070 (-2, +2) |
| nssv14240004 | Submitted genomic | NC_000011.9:g.(147 77860_14777864)_(1 4872614_14872618)i nv174 | GRCh37 (hg19) | NC_000011.9 | Chr11 | 14,777,862 (-2, +2) | 14,872,616 (-2, +2) |