nsv4360622
- Organism: Homo sapiens
- Study:nstd169 (Giner-Delgado et al. 2019)
- Variant Type:inversion
- Method Type:MLPA
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,346
- Publication(s):Giner-Delgado 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: 598 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 599 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360622 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 6,219,006 | 6,219,008 | 6,220,350 | 6,220,351 |
| nsv4360622 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 6,137,047 | 6,137,049 | 6,138,391 | 6,138,392 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607156 | inversion | MLPA | Genotyping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607156 | Remapped | Perfect | NC_000023.11:g.(62 19006_6219008)_(62 20350_6220351)inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 6,219,006 | 6,219,008 | 6,220,350 | 6,220,351 |
| nssv15607156 | Submitted genomic | NC_000023.10:g.(61 37047_6137049)_(61 38391_6138392)inv | GRCh37.p13 | NC_000023.10 | ChrX | 6,137,047 | 6,137,049 | 6,138,391 | 6,138,392 |