nsv3169185
- 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:206,826,356
- 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: 504964 SVs from 155 studies. See in: genome view
Overlapping variant regions from other studies: 504292 SVs from 155 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3169185 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 32,916,404 (-59, +59) | 239,742,759 (-59, +59) |
| nsv3169185 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 33,141,471 (-59, +59) | 240,664,453 (-59, +59) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14239807 | inversion | DB80 | Sequencing | Paired-end mapping | 17 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14239807 | Remapped | Good | NC_000002.12:g.(32 916345_32916463)_( 239742700_23974281 8)inv | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 32,916,404 (-59, +59) | 239,742,759 (-59, +59) |
| nssv14239807 | Submitted genomic | NC_000002.11:g.(33 141412_33141530)_( 240664394_24066451 2)inv | GRCh37 (hg19) | NC_000002.11 | Chr2 | 33,141,471 (-59, +59) | 240,664,453 (-59, +59) |