nsv138179
- 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:9,748
- 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: 96 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 34 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv138179 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 9,605,093 | 9,614,840 |
| nsv138179 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 9,715,769 | 9,725,516 |
| nsv138179 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000019.8 | Chr19 | 9,576,769 | 9,586,516 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv156757 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv156757 | Remapped | Perfect | NC_000019.10:g.960 5093_9614840del974 8 | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 9,605,093 | 9,614,840 |
| nssv156757 | Remapped | Perfect | NC_000019.9:g.9715 769_9725516del9748 | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 9,715,769 | 9,725,516 |
| nssv156757 | Submitted genomic | NC_000019.8:g.9576 769_9586516del9748 | NCBI35 (hg17) | NC_000019.8 | Chr19 | 9,576,769 | 9,586,516 |