nsv823631
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:133,729
- Publication(s):Park 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: 421 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 421 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 102 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv823631 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 98,088,701 | 98,222,429 |
| nsv823631 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 98,554,257 | 98,687,985 |
| nsv823631 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 98,326,845 | 98,460,573 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1440821 | Remapped | Perfect | NC_000001.11:g.(?_ 98088701)_(9822242 9_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 98,088,701 | 98,222,429 |
| nssv1440821 | Remapped | Perfect | NC_000001.10:g.(?_ 98554257)_(9868798 5_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 98,554,257 | 98,687,985 |
| nssv1440821 | Submitted genomic | NC_000001.9:g.(?_9 8326845)_(98460573 _?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 98,326,845 | 98,460,573 |