nsv4360625
- 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:11,374
- 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: 398 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 395 SVs from 37 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360625 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 76,141,868 | 76,146,030 | 76,149,079 | 76,153,241 |
| nsv4360625 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 75,361,703 | 75,365,865 | 75,368,914 | 75,373,076 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607159 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607159 | Remapped | Perfect | NC_000023.11:g.(76 141868_76146030)_( 76149079_76153241) inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 76,141,868 | 76,146,030 | 76,149,079 | 76,153,241 |
| nssv15607159 | Submitted genomic | NC_000023.10:g.(75 361703_75365865)_( 75368914_75373076) inv | GRCh37.p13 | NC_000023.10 | ChrX | 75,361,703 | 75,365,865 | 75,368,914 | 75,373,076 |