nsv481850
- Organism: Homo sapiens
- Study:nstd36 (Mitsui et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:459,262
- Publication(s):Mitsui et al. 2010
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: 2670 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 2670 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 745 SVs from 32 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv481850 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 161,759,091 | 162,218,352 |
| nsv481850 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 162,180,123 | 162,639,384 |
| nsv481850 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 162,100,113 | 162,559,374 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|---|
| nssv650130 | deletion | Oligo aCGH, Sequencing | Probe signal intensity, Sequence alignment | Parkinsonian Disorders | Pathogenic | Submitter |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv650130 | Remapped | Perfect | NC_000006.12:g.161 759091_162218352de l | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 161,759,091 | 162,218,352 |
| nssv650130 | Remapped | Perfect | NC_000006.11:g.162 180123_162639384de l | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 162,180,123 | 162,639,384 |
| nssv650130 | Submitted genomic | NC_000006.10:g.162 100113_162559374de l | NCBI36 (hg18) | NC_000006.10 | Chr6 | 162,100,113 | 162,559,374 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|
| nssv650130 | NCBI36: NC_000006.10:g.162100113_162559374del | deletion | Parkinsonian Disorders | Pathogenic | Submitter |