esv1835752
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:227,586
- Publication(s):Pinto et al. 2011
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: 586 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 586 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 154 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1835752 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 197,826,282 | 198,053,867 |
| esv1835752 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 198,691,006 | 198,918,591 |
| esv1835752 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 198,399,251 | 198,626,836 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4367745 | Remapped | Perfect | NC_000002.12:g.(?_ 197826282)_(198053 867_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 197,826,282 | 198,053,867 |
| essv4367745 | Remapped | Perfect | NC_000002.11:g.(?_ 198691006)_(198918 591_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 198,691,006 | 198,918,591 |
| essv4367745 | Submitted genomic | NC_000002.10:g.(?_ 198399251)_(198626 836_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 198,399,251 | 198,626,836 |