nsv5038830
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:49,985,842
- Publication(s):Abel 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: 116637 SVs from 146 studies. See in: genome view
Overlapping variant regions from other studies: 116139 SVs from 146 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5038830 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 84,210,835 (-6) | 134,196,676 (-6) | ||
| nsv5038830 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 84,920,553 (-6) | 134,517,814 (-6) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16496277 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16496277 | Submitted genomic | NC_000006.12:g.(84 210829_?)_(1341966 70_?)inv | GRCh38 (hg38) | NC_000006.12 | Chr6 | 84,210,835 (-6) | 134,196,676 (-6) | ||
| nssv16496277 | Remapped | Good | NC_000006.11:g.(84 920547_?)_(1345178 08_?)inv | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 84,920,553 (-6) | 134,517,814 (-6) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16496277 | <0.001 | 1 | 29246 |