esv3573133
- Organism: Homo sapiens
- Study:estd212 (Uddin et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:296,230
- Publication(s):Uddin et al. 2014
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: 3116 SVs from 101 studies. See in: genome view
Overlapping variant regions from other studies: 3120 SVs from 101 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3573133 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 11,645,688 | 11,941,917 |
| esv3573133 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 11,645,688 | 11,941,917 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| essv9790417 | copy number loss | SNP array | Probe signal intensity | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv9790417 | Remapped | Perfect | NC_000009.12:g.(?_ 11645688)_(1194191 7_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 11,645,688 | 11,941,917 |
| essv9790417 | Submitted genomic | NC_000009.11:g.(?_ 11645688)_(1194191 7_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 11,645,688 | 11,941,917 |