esv29992
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:826,944
- Publication(s):Levy et al. 2007
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: 6424 SVs from 122 studies. See in: genome view
Overlapping variant regions from other studies: 6460 SVs from 122 studies. See in: genome view
Overlapping variant regions from other studies: 2926 SVs from 34 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29992 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 22,099,274 | 22,926,217 |
| esv29992 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000022.10 | Chr22 | 22,453,684 | 23,268,390 |
| esv29992 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000022.9 | Chr22 | 20,783,684 | 21,598,390 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84231 | Remapped | Good | NC_000022.11:g.(?_ 22099274)_(2292621 7_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 22,099,274 | 22,926,217 |
| essv84231 | Remapped | Perfect | NC_000022.10:g.(?_ 22453684)_(2326839 0_?)dup | GRCh37.p13 | First Pass | NC_000022.10 | Chr22 | 22,453,684 | 23,268,390 |
| essv84231 | Submitted genomic | NC_000022.9:g.(?_2 0783684)_(21598390 _?)dup | NCBI36 (hg18) | NC_000022.9 | Chr22 | 20,783,684 | 21,598,390 |