nsv6105951
- 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:314,122
- 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: 1178 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1183 SVs from 79 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6105951 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 53,740,006 | 54,054,127 | ||
| nsv6105951 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 55,499,766 | 55,813,887 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17595674 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17595674 | Submitted genomic | NC_000010.11:g.537 40006_54054127inv | GRCh38 (hg38) | NC_000010.11 | Chr10 | 53,740,006 | 54,054,127 | ||
| nssv17595674 | Remapped | Perfect | NC_000010.10:g.554 99766_55813887inv | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 55,499,766 | 55,813,887 |