nsv510928
- Organism: Homo sapiens
- Study:nstd49 (Teague et al. 2010)
- Variant Type:complex substitution
- Method Type:Optical mapping
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:20,531
- Publication(s):Teague 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: 303 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 303 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 7 SVs from 1 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv510928 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 174,302,319 | 174,322,849 |
| nsv510928 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 175,223,470 | 175,244,000 |
| nsv510928 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000004.9 | Chr4 | 175,598,200 | 175,618,730 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|---|---|
| nssv624294 | complex substitution | GM18994 | Optical mapping | Optical mapping | 1,936 | |||
| nssv618606 | complex substitution | CHM | Optical mapping | Optical mapping | Hydatidiform Mole | not provided | Submitter | 1,350 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|
| nssv624294 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 174,302,319 | 174,322,849 |
| nssv618606 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 174,304,169 | 174,322,849 |
| nssv624294 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 175,223,470 | 175,244,000 |
| nssv618606 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 175,225,320 | 175,244,000 |
| nssv624294 | Submitted genomic | NCBI35 (hg17) | NC_000004.9 | Chr4 | 175,598,200 | 175,618,730 | ||
| nssv618606 | Submitted genomic | NCBI35 (hg17) | NC_000004.9 | Chr4 | 175,600,050 | 175,618,730 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | Sample ID | Type | Subject Phenotype | Clinical Interpretation | Source of Interpretation | Gender | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|---|
| nssv618606 | CHM | complex substitution | Hydatidiform Mole | not provided | Submitter | Female | 1,350 |