nsv1078895
- Organism: Homo sapiens
- Study:nstd99 (Thareja et al. 2015)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:12,803
- Publication(s):Thareja et al. 2015
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 366 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 366 SVs from 45 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1078895 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 2,920,319 | 2,933,121 |
| nsv1078895 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 2,962,003 | 2,974,805 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3766894 | inversion | KWP1 | Sequencing | Read depth and paired-end mapping | 11,116 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3766894 | Remapped | Perfect | NC_000003.12:g.292 0319_2933121inv | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 2,920,319 | 2,933,121 |
| nssv3766894 | Submitted genomic | NC_000003.11:g.296 2003_2974805inv | GRCh37 (hg19) | NC_000003.11 | Chr3 | 2,962,003 | 2,974,805 |