nsv4360634
- 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:9,331
- 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: 244 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 51 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4360634 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 310,225 | 311,836 | 317,945 | 319,555 |
nsv4360634 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000011.9 | Chr11 | 310,225 | 311,836 | 317,945 | 319,555 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15607144 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15607144 | Remapped | Perfect | NC_000011.10:g.(31 0225_311836)_(3179 45_319555)inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 310,225 | 311,836 | 317,945 | 319,555 |
nssv15607144 | Submitted genomic | NC_000011.9:g.(310 225_311836)_(31794 5_319555)inv | GRCh37.p13 | NC_000011.9 | Chr11 | 310,225 | 311,836 | 317,945 | 319,555 |