nsv1929
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:26,837
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 509 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 509 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 9 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1929 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 89,601,681 | 89,628,517 |
| nsv1929 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 89,668,089 | 89,694,925 |
| nsv1929 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 88,195,590 | 88,222,426 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv5624 | Remapped | Perfect | NC_000016.10:g.(89 601681_?)_(?_89628 517)ins6328 | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 89,601,681 | 89,628,517 |
| nssv5624 | Remapped | Perfect | NC_000016.9:g.(896 68089_?)_(?_896949 25)ins6328 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 89,668,089 | 89,694,925 |
| nssv5624 | Submitted genomic | NC_000016.8:g.(881 95590_?)_(?_882224 26)ins6328 | NCBI35 (hg17) | NC_000016.8 | Chr16 | 88,195,590 | 88,222,426 |