nsv4657992
- 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:26,074
- 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: 405 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 406 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4657992 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000024.10 | ChrY | 21,021,692 | 21,047,765 | ||
| nsv4657992 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 23,183,578 | 23,209,651 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16181399 | inversion | ddPCR | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16181399 | Submitted genomic | NC_000024.10:g.(?_ 21021692)_(2104776 5_?)inv | GRCh38.p13 | NC_000024.10 | ChrY | 21,021,692 | 21,047,765 | ||
| nssv16181399 | Remapped | Perfect | NC_000024.9:g.(?_2 3183578)_(23209651 _?)inv | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 23,183,578 | 23,209,651 |