nsv4360639
- 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:2,984
- 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: 160 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 156 SVs from 40 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360639 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 106,720,678 | 106,721,331 | 106,723,006 | 106,723,661 |
| nsv4360639 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000006.11 | Chr6 | 107,168,553 | 107,169,206 | 107,170,881 | 107,171,536 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607180 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607180 | Remapped | Perfect | NC_000006.12:g.(10 6720678_106721331) _(106723006_106723 661)inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 106,720,678 | 106,721,331 | 106,723,006 | 106,723,661 |
| nssv15607180 | Submitted genomic | NC_000006.11:g.(10 7168553_107169206) _(107170881_107171 536)inv | GRCh37.p13 | NC_000006.11 | Chr6 | 107,168,553 | 107,169,206 | 107,170,881 | 107,171,536 |