nsv4360643
- 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:255
- 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: 158 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 158 SVs from 39 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360643 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 74,283,223 | 74,283,224 | 74,283,474 | 74,283,477 |
| nsv4360643 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000009.11 | Chr9 | 76,898,139 | 76,898,140 | 76,898,390 | 76,898,393 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607175 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607175 | Remapped | Perfect | NC_000009.12:g.(74 283223_74283224)_( 74283474_74283477) inv | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 74,283,223 | 74,283,224 | 74,283,474 | 74,283,477 |
| nssv15607175 | Submitted genomic | NC_000009.11:g.(76 898139_76898140)_( 76898390_76898393) inv | GRCh37.p13 | NC_000009.11 | Chr9 | 76,898,139 | 76,898,140 | 76,898,390 | 76,898,393 |