nsv437877
- Organism: Homo sapiens
- Study:nstd20 (McCarroll et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:67,134
- Publication(s):McCarroll et al. 2006
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: 253 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 253 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv437877 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 104,991,981 | 105,059,114 |
| nsv437877 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 104,710,825 | 104,777,958 |
| nsv437877 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000003.8 | Chr3 | 106,031,726 | 106,098,859 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv471353 | Remapped | Perfect | NC_000003.12:g.(?_ 104991981)_(105059 114_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 104,991,981 | 105,059,114 |
| nssv471353 | Remapped | Perfect | NC_000003.11:g.(?_ 104710825)_(104777 958_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 104,710,825 | 104,777,958 |
| nssv471353 | Submitted genomic | NC_000003.8:g.(?_1 06031726)_(1060988 59_?)del | NCBI34 (hg16) | NC_000003.8 | Chr3 | 106,031,726 | 106,098,859 |