nsv81420
- 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: 92 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 92 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv81420 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 57,892,656 | 57,892,656 |
| nsv81420 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 58,359,374 | 58,359,374 |
| nsv81420 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000014.7 | Chr14 | 57,429,127 | 57,429,127 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv99998 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv99998 | Remapped | Perfect | NC_000014.9:g.5789 2656_57892657insT | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 57,892,656 | 57,892,656 |
| nssv99998 | Remapped | Perfect | NC_000014.8:g.5835 9374_58359375insT | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 58,359,374 | 58,359,374 |
| nssv99998 | Submitted genomic | NC_000014.7:g.5742 9127_57429128insT | NCBI35 (hg17) | NC_000014.7 | Chr14 | 57,429,127 | 57,429,127 |