esv2763324
- 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:94,512
- 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: 414 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 414 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2763324 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 164,978,854 | 165,073,365 |
| esv2763324 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 164,696,642 | 164,791,153 |
| esv2763324 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 166,179,336 | 166,273,847 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7028152 | copy number gain | SW_1074 | SNP array | SNP genotyping analysis | 37 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv7028152 | Remapped | Perfect | NC_000003.12:g.(?_ 164978854)_(165073 365_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 164,978,854 | 165,073,365 |
| essv7028152 | Remapped | Perfect | NC_000003.11:g.(?_ 164696642)_(164791 153_?)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 164,696,642 | 164,791,153 |
| essv7028152 | Submitted genomic | NC_000003.10:g.(?_ 166179336)_(166273 847_?)dup | NCBI36 (hg18) | NC_000003.10 | Chr3 | 166,179,336 | 166,273,847 |