esv991867
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:32,943
- 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: 992 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 992 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 642 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv991867 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 1,580,305 | 1,613,247 |
| esv991867 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 1,560,951 | 1,593,893 |
| esv991867 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 1,508,951 | 1,541,893 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586018 | Remapped | Perfect | NC_000020.11:g.(?_ 1580305)_(1613247_ ?)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 1,580,305 | 1,613,247 |
| essv3586018 | Remapped | Perfect | NC_000020.10:g.(?_ 1560951)_(1593893_ ?)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 1,560,951 | 1,593,893 |
| essv3586018 | Submitted genomic | NC_000020.9:g.(?_1 508951)_(1541893_? )dup | NCBI36 (hg18) | NC_000020.9 | Chr20 | 1,508,951 | 1,541,893 |