nsv4360656
- 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:8,076
- 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: 588 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 588 SVs from 62 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360656 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 187,948,441 | 187,949,937 | 187,955,020 | 187,956,516 |
| nsv4360656 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000004.11 | Chr4 | 188,869,595 | 188,871,091 | 188,876,174 | 188,877,670 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607166 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607166 | Remapped | Perfect | NC_000004.12:g.(18 7948441_187949937) _(187955020_187956 516)inv | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 187,948,441 | 187,949,937 | 187,955,020 | 187,956,516 |
| nssv15607166 | Submitted genomic | NC_000004.11:g.(18 8869595_188871091) _(188876174_188877 670)inv | GRCh37.p13 | NC_000004.11 | Chr4 | 188,869,595 | 188,871,091 | 188,876,174 | 188,877,670 |