nsv6109072
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:84,113
- Publication(s):Wu et al. 2021
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: 332 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 340 SVs from 58 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6109072 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 63,982,028 | 64,066,140 | ||
| nsv6109072 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 63,442,406 | 63,526,518 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17567351 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17567351 | Submitted genomic | NC_000007.14:g.639 82028_64066140inv | GRCh38 (hg38) | NC_000007.14 | Chr7 | 63,982,028 | 64,066,140 | ||
| nssv17567351 | Remapped | Perfect | NC_000007.13:g.634 42406_63526518inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 63,442,406 | 63,526,518 |