nsv1132999
- Organism: Homo sapiens
- Study:nstd106 (Alsmadi et al. 2014)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:87,747,463
- Publication(s):Alsmadi et al. 2014
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: 229112 SVs from 157 studies. See in: genome view
Overlapping variant regions from other studies: 229177 SVs from 157 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1132999 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,599,278 | 89,346,740 |
| nsv1132999 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 1,620,508 | 89,079,908 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3987796 | inversion | KWS1 | Sequencing | Read depth and paired-end mapping | 22,470 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3987796 | Remapped | Good | NC_000011.10:g.(15 99278_?)_(?_893467 40)inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,599,278 | 89,346,740 |
| nssv3987796 | Submitted genomic | NC_000011.9:g.(162 0508_?)_(?_8907990 8)inv | GRCh37 (hg19) | NC_000011.9 | Chr11 | 1,620,508 | 89,079,908 |