nsv3960077
- 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:160,565
- 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: 1007 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1007 SVs from 85 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3960077 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 167,198,373 | 167,358,937 | ||
| nsv3960077 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 167,611,861 | 167,772,425 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15222542 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv15222542 | Submitted genomic | NC_000006.12:g.(16 7198373_?)_(?_1673 58937)inv | GRCh38 (hg38) | NC_000006.12 | Chr6 | 167,198,373 | 167,358,937 | ||
| nssv15222542 | Remapped | Perfect | NC_000006.11:g.(16 7611861_?)_(?_1677 72425)inv | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 167,611,861 | 167,772,425 |