nsv4360647
- 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:7,893
- 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: 327 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 327 SVs from 55 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360647 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 181,095,750 | 181,098,580 | 181,100,851 | 181,103,642 |
| nsv4360647 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000005.9 | Chr5 | 180,522,750 | 180,525,580 | 180,527,851 | 180,530,642 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607183 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607183 | Remapped | Perfect | NC_000005.10:g.(18 1095750_181098580) _(181100851_181103 642)inv | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 181,095,750 | 181,098,580 | 181,100,851 | 181,103,642 |
| nssv15607183 | Submitted genomic | NC_000005.9:g.(180 522750_180525580)_ (180527851_1805306 42)inv | GRCh37.p13 | NC_000005.9 | Chr5 | 180,522,750 | 180,525,580 | 180,527,851 | 180,530,642 |