nsv393922
- 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: 259 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 259 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 5 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv393922 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 19,939,266 | 19,939,266 |
| nsv393922 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 19,796,777 | 19,796,777 |
| nsv393922 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 19,841,057 | 19,841,057 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv412500 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv412500 | Remapped | Perfect | NC_000008.11:g.199 39266_19939267insC C | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 19,939,266 | 19,939,266 |
| nssv412500 | Remapped | Perfect | NC_000008.10:g.197 96777_19796778insC C | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 19,796,777 | 19,796,777 |
| nssv412500 | Submitted genomic | NC_000008.9:g.1984 1057_19841058insCC | NCBI35 (hg17) | NC_000008.9 | Chr8 | 19,841,057 | 19,841,057 |