nsv3169329
- 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:37,504
- 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: 467 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 461 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3169329 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 37,685,205 (-6, +6) | 37,722,708 (-6, +6) |
| nsv3169329 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 37,544,458 (-6, +6) | 37,581,961 (-6, +6) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14240106 | inversion | DB73 | Sequencing | Paired-end mapping | 31 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14240106 | Remapped | Perfect | NC_000023.11:g.(37 685199_37685211)_( 37722702_37722714) inv102 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 37,685,205 (-6, +6) | 37,722,708 (-6, +6) |
| nssv14240106 | Submitted genomic | NC_000023.10:g.(37 544452_37544464)_( 37581955_37581967) inv102 | GRCh37 (hg19) | NC_000023.10 | ChrX | 37,544,458 (-6, +6) | 37,581,961 (-6, +6) |