nsv4360612
- 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:1,904
- 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: 374 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 374 SVs from 70 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360612 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 187,495,697 | 187,497,346 | 187,497,596 | 187,497,600 |
| nsv4360612 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000001.10 | Chr1 | 187,464,829 | 187,466,478 | 187,466,728 | 187,466,732 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607164 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607164 | Remapped | Perfect | NC_000001.11:g.(18 7495697_187497346) _(187497596_187497 600)inv | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 187,495,697 | 187,497,346 | 187,497,596 | 187,497,600 |
| nssv15607164 | Submitted genomic | NC_000001.10:g.(18 7464829_187466478) _(187466728_187466 732)inv | GRCh37.p13 | NC_000001.10 | Chr1 | 187,464,829 | 187,466,478 | 187,466,728 | 187,466,732 |