nsv112105
- Organism: Homo sapiens
- Study:nstd6 (Mills et al. 2006)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,611
- 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: 134 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv112105 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 65,038,711 | 65,048,321 |
| nsv112105 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 63,034,829 | 63,044,439 |
| nsv112105 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000017.9 | Chr17 | 60,465,291 | 60,474,901 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv130683 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv130683 | Remapped | Perfect | NC_000017.11:g.650 38711_65048321del9 611 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,038,711 | 65,048,321 |
| nssv130683 | Remapped | Perfect | NC_000017.10:g.630 34829_63044439del9 611 | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,034,829 | 63,044,439 |
| nssv130683 | Submitted genomic | NC_000017.9:g.6046 5291_60474901del96 11 | NCBI35 (hg17) | NC_000017.9 | Chr17 | 60,465,291 | 60,474,901 |