nsv4360619
- 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:56,036
- 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: 663 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 653 SVs from 50 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360619 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 154,338,058 | 154,338,058 | 154,394,093 | 154,394,093 |
| nsv4360619 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 153,566,408 | 153,575,614 | 153,613,228 | 153,622,435 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607162 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607162 | Remapped | Good | NC_000023.11:g.(15 4338058_154338058) _(154394093_154394 093)inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 154,338,058 | 154,338,058 | 154,394,093 | 154,394,093 |
| nssv15607162 | Submitted genomic | NC_000023.10:g.(15 3566408_153575614) _(153613228_153622 435)inv | GRCh37.p13 | NC_000023.10 | ChrX | 153,566,408 | 153,575,614 | 153,613,228 | 153,622,435 |