esv2761468
- Organism: Homo sapiens
- Study:estd203 (Vogler 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:2,007
- Publication(s):Vogler 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: 222 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 222 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 73 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2761468 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 125,533,955 | 125,535,961 |
| esv2761468 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 126,546,197 | 126,548,203 |
| esv2761468 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 126,615,379 | 126,617,385 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv6993403 | copy number loss | SW_1103 | SNP array | SNP genotyping analysis | 43 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv6993403 | Remapped | Perfect | NC_000008.11:g.(?_ 125533955)_(125535 961_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 125,533,955 | 125,535,961 |
| essv6993403 | Remapped | Perfect | NC_000008.10:g.(?_ 126546197)_(126548 203_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 126,546,197 | 126,548,203 |
| essv6993403 | Submitted genomic | NC_000008.9:g.(?_1 26615379)_(1266173 85_?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 126,615,379 | 126,617,385 |