esv3693263
- 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:16,815
- 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: 252 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 252 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 99 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3693263 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 12,412,475 | 12,429,289 |
| esv3693263 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 12,523,289 | 12,540,103 |
| esv3693263 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 12,384,289 | 12,401,103 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16509331 | Remapped | Perfect | NC_000019.10:g.(?_ 12412475)_(1242928 9_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 12,412,475 | 12,429,289 |
| essv16509331 | Remapped | Perfect | NC_000019.9:g.(?_1 2523289)_(12540103 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 12,523,289 | 12,540,103 |
| essv16509331 | Submitted genomic | NC_000019.8:g.(?_1 2384289)_(12401103 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 12,384,289 | 12,401,103 |