nsv3167831
- Organism: Homo sapiens
- Study:nstd158 (Cleal et al. 2019)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:173,255,573
- Publication(s):Cleal et al. 2019
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: 416237 SVs from 155 studies. See in: genome view
Overlapping variant regions from other studies: 415643 SVs from 155 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3167831 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 32,867,019 (-389, +389) | 206,122,591 (-389, +389) |
| nsv3167831 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 33,092,086 (-389, +389) | 206,987,315 (-389, +389) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14239794 | inversion | DB47 | Sequencing | Paired-end mapping | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14239794 | Remapped | Good | NC_000002.12:g.(32 866630_32867408)_( 206122202_20612298 0)inv | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 32,867,019 (-389, +389) | 206,122,591 (-389, +389) |
| nssv14239794 | Submitted genomic | NC_000002.11:g.(33 091697_33092475)_( 206986926_20698770 4)inv | GRCh37 (hg19) | NC_000002.11 | Chr2 | 33,092,086 (-389, +389) | 206,987,315 (-389, +389) |