esv993767
- Organism: Homo sapiens
- Study:estd180 (Pang 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:48,850
- Publication(s):Pang 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: 287 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 327 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 184 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv993767 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 67,501,012 | 67,549,861 |
| esv993767 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 65,869,511 | 65,918,360 |
| esv993767 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 65,609,331 | 65,658,180 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586403 | Remapped | Perfect | NC_000009.12:g.(?_ 67501012)_(6754986 1_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 67,501,012 | 67,549,861 |
| essv3586403 | Remapped | Perfect | NC_000009.11:g.(?_ 65869511)_(6591836 0_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 65,869,511 | 65,918,360 |
| essv3586403 | Submitted genomic | NC_000009.10:g.(?_ 65609331)_(6565818 0_?)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 65,609,331 | 65,658,180 |