nsv4360628
- 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:17,678
- 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: 281 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 281 SVs from 56 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360628 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 75,205,642 | 75,206,200 | 75,222,761 | 75,223,319 |
| nsv4360628 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000016.9 | Chr16 | 75,239,540 | 75,240,098 | 75,256,659 | 75,257,217 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607150 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607150 | Remapped | Perfect | NC_000016.10:g.(75 205642_75206200)_( 75222761_75223319) inv | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 75,205,642 | 75,206,200 | 75,222,761 | 75,223,319 |
| nssv15607150 | Submitted genomic | NC_000016.9:g.(752 39540_75240098)_(7 5256659_75257217)i nv | GRCh37.p13 | NC_000016.9 | Chr16 | 75,239,540 | 75,240,098 | 75,256,659 | 75,257,217 |