nsv4658009
- Organism: Homo sapiens
- Study:nstd185 (Puig et al. 2020)
- Variant Type:inversion
- Method Type:ddPCR
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35,035
- Publication(s):Puig et al. 2020
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: 717 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 811 SVs from 81 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4658009 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000008.11 | Chr8 | 2,343,351 | 2,378,385 | ||
| nsv4658009 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 2,292,235 | 2,322,202 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16181387 | inversion | ddPCR | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16181387 | Submitted genomic | NC_000008.11:g.(?_ 2343351)_(2378385_ ?)inv | GRCh38.p13 | NC_000008.11 | Chr8 | 2,343,351 | 2,378,385 | ||
| nssv16181387 | Remapped | Pass | NC_000008.10:g.(?_ 2292235)_(2322202_ ?)inv | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 2,292,235 | 2,322,202 |