nsv3167844
- 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:27,874
- 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: 211 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 211 SVs from 27 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3167844 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 78,847,781 (-324, +324) | 78,875,654 (-324, +324) |
| nsv3167844 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 76,843,863 (-324, +324) | 76,871,736 (-324, +324) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14240092 | inversion | DB79 | Sequencing | Paired-end mapping | 61 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14240092 | Remapped | Perfect | NC_000017.11:g.(78 847457_78848105)_( 78875330_78875978) inv | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 78,847,781 (-324, +324) | 78,875,654 (-324, +324) |
| nssv14240092 | Submitted genomic | NC_000017.10:g.(76 843539_76844187)_( 76871412_76872060) inv | GRCh37 (hg19) | NC_000017.10 | Chr17 | 76,843,863 (-324, +324) | 76,871,736 (-324, +324) |