esv2758656
- Organism: Homo sapiens
- Study:estd1 (Redon et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:252,406
- Publication(s):Redon et al. 2006
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: 1174 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1174 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 47 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2758656 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 74,300,882 | 74,553,287 |
| esv2758656 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 74,334,780 | 74,587,185 |
| esv2758656 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 72,892,281 | 73,144,686 |
Variant Call Information
| Variant Call ID | Type | Method |
|---|---|---|
| esv2758431 | copy number variation | Merged region |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| esv2758431 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 74,300,882 | 74,553,287 |
| esv2758431 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 74,334,780 | 74,587,185 |
| esv2758431 | Submitted genomic | NCBI35 (hg17) | NC_000016.8 | Chr16 | 72,892,281 | 73,144,686 |