nsv433361
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:132,008
- Publication(s):Cooper et al. 2008
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: 1066 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1066 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 10 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433361 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 130,058,958 | 130,190,965 |
| nsv433361 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 129,777,801 | 129,909,808 |
| nsv433361 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000003.9 | Chr3 | 131,260,499 | 131,392,506 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463242 | Remapped | Perfect | NC_000003.12:g.(?_ 130058958)_(130190 965_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 130,058,958 | 130,190,965 |
| nssv463242 | Remapped | Perfect | NC_000003.11:g.(?_ 129777801)_(129909 808_?)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 129,777,801 | 129,909,808 |
| nssv463242 | Submitted genomic | NC_000003.9:g.(?_1 31260499)_(1313925 06_?)dup | NCBI35 (hg17) | NC_000003.9 | Chr3 | 131,260,499 | 131,392,506 |