esv3693212
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:150,299
- Publication(s):Palta et al. 2015
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: 1230 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 1230 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 512 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3693212 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 99,817,230 | 99,967,528 |
| esv3693212 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 100,357,435 | 100,507,733 |
| esv3693212 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 98,174,958 | 98,325,256 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16508526 | Remapped | Perfect | NC_000015.10:g.(?_ 99817230)_(9996752 8_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 99,817,230 | 99,967,528 |
| essv16508526 | Remapped | Perfect | NC_000015.9:g.(?_1 00357435)_(1005077 33_?)dup | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 100,357,435 | 100,507,733 |
| essv16508526 | Submitted genomic | NC_000015.8:g.(?_9 8174958)_(98325256 _?)dup | NCBI36 (hg18) | NC_000015.8 | Chr15 | 98,174,958 | 98,325,256 |