nsv7137157
- Organism: Homo sapiens
- Study:nstd234 (Chandrasekhar et al. 2023)
- Variant Type:inversion
- Method Type:Karyotyping
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:51,456,708
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: 68888 SVs from 109 studies. See in: genome view
Overlapping variant regions from other studies: 68672 SVs from 109 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7137157 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 31,608,425 | 83,065,132 |
| nsv7137157 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 31,626,542 | 82,320,140 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv18830932 | inversion | DMD1 | Karyotyping | Manual observation |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18830932 | Remapped | Good | NC_000023.11:g.316 08425_83065132inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 31,608,425 | 83,065,132 |
| nssv18830932 | Submitted genomic | NC_000023.10:g.316 26542_82320140inv | GRCh37 (hg19) | NC_000023.10 | ChrX | 31,626,542 | 82,320,140 |