nsv481696
- 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:229,588
- 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: 1191 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1191 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 307 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv481696 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 161,750,689 | 161,980,276 |
| nsv481696 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 162,171,721 | 162,401,308 |
| nsv481696 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 162,091,711 | 162,321,298 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|---|
| nssv649976 | duplication | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv649976 | Remapped | Perfect | NC_000006.12:g.161 750689_161980276du p | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 161,750,689 | 161,980,276 |
| nssv649976 | Remapped | Perfect | NC_000006.11:g.162 171721_162401308du p | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 162,171,721 | 162,401,308 |
| nssv649976 | Submitted genomic | NC_000006.10:g.162 091711_162321298du p | NCBI36 (hg18) | NC_000006.10 | Chr6 | 162,091,711 | 162,321,298 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|
| nssv649976 | NCBI36: NC_000006.10:g.162091711_162321298dup | duplication | Parkinsonian Disorders | Pathogenic | Submitter |