nsv3961084
- 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:1,196,866
- 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: 4426 SVs from 99 studies. See in: genome view
Overlapping variant regions from other studies: 4426 SVs from 99 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3961084 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000019.10 | Chr19 | 36,102,738 | 37,299,603 | ||
| nsv3961084 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 36,593,640 | 37,790,505 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15210999 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv15210999 | Submitted genomic | NC_000019.10:g.(36 102738_?)_(?_37299 603)inv | GRCh38 (hg38) | NC_000019.10 | Chr19 | 36,102,738 | 37,299,603 | ||
| nssv15210999 | Remapped | Perfect | NC_000019.9:g.(365 93640_?)_(?_377905 05)inv | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 36,593,640 | 37,790,505 |