nsv4657997
- 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:165,607
- 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: 701 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 806 SVs from 74 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4657997 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000020.11 | Chr20 | 25,845,152 | 26,010,758 | ||
| nsv4657997 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 25,825,788 | 25,991,394 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16181392 | inversion | ddPCR | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16181392 | Submitted genomic | NC_000020.11:g.(?_ 25845152)_(2601075 8_?)inv | GRCh38.p13 | NC_000020.11 | Chr20 | 25,845,152 | 26,010,758 | ||
| nssv16181392 | Remapped | Perfect | NC_000020.10:g.(?_ 25825788)_(2599139 4_?)inv | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 25,825,788 | 25,991,394 |