nsv3168776
- 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:24,536,825
- 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: 64645 SVs from 142 studies. See in: genome view
Overlapping variant regions from other studies: 64853 SVs from 142 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3168776 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 37,053,223 (-2, +2) | 61,590,047 (-2, +2) |
| nsv3168776 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 37,074,773 (-2, +2) | 61,357,519 (-2, +2) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14240036 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv14240036 | Remapped | Good | NC_000011.10:g.(37 053221_37053225)_( 61590045_61590049) inv157 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 37,053,223 (-2, +2) | 61,590,047 (-2, +2) |
| nssv14240036 | Submitted genomic | NC_000011.9:g.(370 74771_37074775)_(6 1357517_61357521)i nv157 | GRCh37 (hg19) | NC_000011.9 | Chr11 | 37,074,773 (-2, +2) | 61,357,519 (-2, +2) |