nsv4360644
- 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:14,048
- 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: 236 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 60 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360644 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 113,105,263 | 113,111,686 | 113,112,887 | 113,119,310 |
| nsv4360644 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000009.11 | Chr9 | 115,867,543 | 115,873,966 | 115,875,167 | 115,881,590 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607142 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607142 | Remapped | Perfect | NC_000009.12:g.(11 3105263_113111686) _(113112887_113119 310)inv | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 113,105,263 | 113,111,686 | 113,112,887 | 113,119,310 |
| nssv15607142 | Submitted genomic | NC_000009.11:g.(11 5867543_115873966) _(115875167_115881 590)inv | GRCh37.p13 | NC_000009.11 | Chr9 | 115,867,543 | 115,873,966 | 115,875,167 | 115,881,590 |