nsv930460
- Organism: Homo sapiens
- Study:nstd76 (Watson et al. 2013)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2
- Publication(s):Watson et al. 2013
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 2222 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1999 SVs from 77 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv930460 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 106,348,408 | 106,348,409 |
| nsv930460 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 106,804,332 | 106,804,333 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1607657 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1607657 | Remapped | Perfect | NC_000014.9:g.(106 348408_?)_(?_10634 8409)ins49200 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 106,348,408 | 106,348,409 |
| nssv1607657 | Submitted genomic | NC_000014.8:g.(106 804332_?)_(?_10680 4333)ins49200 | GRCh37 (hg19) | NC_000014.8 | Chr14 | 106,804,332 | 106,804,333 |