nsv426259
- Organism: Homo sapiens
- Study:nstd6 (Mills et al. 2006)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Mills et al. 2006
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 370 SVs from 17 studies. See in: genome view
Overlapping variant regions from other studies: 371 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv426259 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 56,856,710 | 56,856,710 |
| nsv426259 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 59,002,857 | 59,002,857 |
| nsv426259 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000024.7 | ChrY | 57,340,982 | 57,340,982 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv444837 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv444837 | Remapped | Perfect | NC_000024.10:g.568 56710_56856711insA GA | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 56,856,710 | 56,856,710 |
| nssv444837 | Remapped | Perfect | NC_000024.9:g.5900 2857_59002858insAG A | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 59,002,857 | 59,002,857 |
| nssv444837 | Submitted genomic | NC_000024.7:g.5734 0982_57340983insAG A | NCBI35 (hg17) | NC_000024.7 | ChrY | 57,340,982 | 57,340,982 |