nsv1068321
- 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:3,063,273
- 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: 7478 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 7478 SVs from 106 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1068321 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 29,675,386 | 32,738,658 |
| nsv1068321 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 29,715,002 | 32,778,270 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3773039 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3773039 | Remapped | Perfect | NC_000007.14:g.296 75386_32738658inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 29,675,386 | 32,738,658 |
| nssv3773039 | Submitted genomic | NC_000007.13:g.297 15002_32778270inv | GRCh37 (hg19) | NC_000007.13 | Chr7 | 29,715,002 | 32,778,270 |