nsv3168810
- 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:80,675,533
- 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: 201076 SVs from 149 studies. See in: genome view
Overlapping variant regions from other studies: 201088 SVs from 149 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3168810 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 115,641,516 (-6, +6) | 196,317,048 (-6, +6) |
| nsv3168810 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 115,360,363 (-6, +6) | 196,043,919 (-6, +6) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14239826 | inversion | DB92 | Sequencing | Paired-end mapping | 14 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14239826 | Remapped | Good | NC_000003.12:g.(11 5641510_115641522) _(196317042_196317 054)inv180 | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 115,641,516 (-6, +6) | 196,317,048 (-6, +6) |
| nssv14239826 | Submitted genomic | NC_000003.11:g.(11 5360357_115360369) _(196043913_196043 925)inv180 | GRCh37 (hg19) | NC_000003.11 | Chr3 | 115,360,363 (-6, +6) | 196,043,919 (-6, +6) |