nsv4360655
- 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:2,034
- 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: 131 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 36 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360655 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 40,233,407 | 40,233,408 | 40,235,439 | 40,235,440 |
| nsv4360655 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000004.11 | Chr4 | 40,235,027 | 40,235,028 | 40,237,059 | 40,237,060 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607186 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607186 | Remapped | Perfect | NC_000004.12:g.(40 233407_40233408)_( 40235439_40235440) inv | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 40,233,407 | 40,233,408 | 40,235,439 | 40,235,440 |
| nssv15607186 | Submitted genomic | NC_000004.11:g.(40 235027_40235028)_( 40237059_40237060) inv | GRCh37.p13 | NC_000004.11 | Chr4 | 40,235,027 | 40,235,028 | 40,237,059 | 40,237,060 |