nsv6108932
- 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:4,996,782
- 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: 14279 SVs from 122 studies. See in: genome view
Overlapping variant regions from other studies: 14294 SVs from 122 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6108932 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 33,574,222 | 38,571,003 | ||
| nsv6108932 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 33,574,220 | 38,571,000 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17585686 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17585686 | Submitted genomic | NC_000009.12:g.335 74222_38571003inv | GRCh38 (hg38) | NC_000009.12 | Chr9 | 33,574,222 | 38,571,003 | ||
| nssv17585686 | Remapped | Perfect | NC_000009.11:g.335 74220_38571000inv | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 33,574,220 | 38,571,000 |