nsv3167759
- 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:41,943,684
- 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: 108701 SVs from 139 studies. See in: genome view
Overlapping variant regions from other studies: 107671 SVs from 139 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3167759 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 24,114,605 (-415, +415) | 66,058,288 (-415, +415) |
| nsv3167759 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 24,267,539 (-415, +415) | 66,452,068 (-415, +415) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14240022 | inversion | DB37 | Sequencing | Paired-end mapping | 28 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14240022 | Remapped | Good | NC_000012.12:g.(24 114190_24115020)_( 66057873_66058703) inv172 | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 24,114,605 (-415, +415) | 66,058,288 (-415, +415) |
| nssv14240022 | Submitted genomic | NC_000012.11:g.(24 267124_24267954)_( 66451653_66452483) inv172 | GRCh37 (hg19) | NC_000012.11 | Chr12 | 24,267,539 (-415, +415) | 66,452,068 (-415, +415) |