nsv4360626
- 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:18,702
- 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: 453 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 450 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360626 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 101,597,544 | 101,597,544 | 101,616,245 | 101,616,245 |
| nsv4360626 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 100,852,522 | 100,857,177 | 100,866,580 | 100,871,235 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607160 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607160 | Remapped | Good | NC_000023.11:g.(10 1597544_101597544) _(101616245_101616 245)inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 101,597,544 | 101,597,544 | 101,616,245 | 101,616,245 |
| nssv15607160 | Submitted genomic | NC_000023.10:g.(10 0852522_100857177) _(100866580_100871 235)inv | GRCh37.p13 | NC_000023.10 | ChrX | 100,852,522 | 100,857,177 | 100,866,580 | 100,871,235 |