nsv6107847
- 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:2,193,915
- 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: 8596 SVs from 123 studies. See in: genome view
Overlapping variant regions from other studies: 7469 SVs from 123 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6107847 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 100,184,978 | 102,378,892 | ||
| nsv6107847 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 99,782,601 | 101,718,950 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17574952 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17574952 | Submitted genomic | NC_000007.14:g.100 184978_102378892in v | GRCh38 (hg38) | NC_000007.14 | Chr7 | 100,184,978 | 102,378,892 | ||
| nssv17574952 | Remapped | Pass | NC_000007.13:g.997 82601_101718950inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 99,782,601 | 101,718,950 |