nsv471688
- Organism: Homo sapiens
- Study:nstd32 (Sharp et al. 2005)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:170,406
- Publication(s):Sharp et al. 2005
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: 1273 SVs from 107 studies. See in: genome view
Overlapping variant regions from other studies: 1273 SVs from 107 studies. See in: genome view
Overlapping variant regions from other studies: 5 SVs from 2 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv471688 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 105,444,910 | 105,615,315 |
| nsv471688 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 105,987,532 | 106,157,937 |
| nsv471688 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000001.7 | Chr1 | 105,342,185 | 105,512,590 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv550647 | Remapped | Perfect | NC_000001.11:g.(?_ 105444910)_(105615 315_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 105,444,910 | 105,615,315 |
| nssv550647 | Remapped | Perfect | NC_000001.10:g.(?_ 105987532)_(106157 937_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 105,987,532 | 106,157,937 |
| nssv550647 | Submitted genomic | NC_000001.7:g.(?_1 05342185)_(1055125 90_?)del | NCBI34 (hg16) | NC_000001.7 | Chr1 | 105,342,185 | 105,512,590 |