nsv3967776
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:inversion
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,458
- Publication(s):Levy-Sakin 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: 269 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 261 SVs from 52 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3967776 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000021.9 | Chr21 | 13,972,490 | 13,993,947 | ||
| nsv3967776 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 15,344,811 | 15,366,268 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15206901 | inversion | Optical mapping | Optical mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15206901 | Submitted genomic | NC_000021.9:g.(139 72490_?)_(?_139939 47)inv | GRCh38 (hg38) | NC_000021.9 | Chr21 | 13,972,490 | 13,993,947 | ||
| nssv15206901 | Remapped | Perfect | NC_000021.8:g.(153 44811_?)_(?_153662 68)inv | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 15,344,811 | 15,366,268 |