nsv4730164
- Organism: Homo sapiens
- Study:nstd198 (Hanlon et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,007
- Publication(s):Hanlon 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: 241 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 247 SVs from 57 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4730164 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000020.11 | Chr20 | 26,077,606 | 26,086,612 | ||
| nsv4730164 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 26,058,242 | 26,067,248 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Zygosity | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| nssv16257128 | inversion | SAMN00006580 | Sequencing | Genotyping | Heterozygous | 344 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16257128 | Submitted genomic | NC_000020.11:g.260 77606_26086612inv | GRCh38 (hg38) | NC_000020.11 | Chr20 | 26,077,606 | 26,086,612 | ||
| nssv16257128 | Remapped | Perfect | NC_000020.10:g.260 58242_26067248inv | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 26,058,242 | 26,067,248 |