esv2757764
- 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:324,286
- 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: 1137 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1137 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 32 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757764 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 195,286,797 | 195,611,082 |
| esv2757764 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 195,255,927 | 195,580,212 |
| esv2757764 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 191,987,584 | 192,311,869 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv11638 | Remapped | Perfect | NC_000001.11:g.(?_ 195286797)_(195611 082_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 195,286,797 | 195,611,082 |
| essv11638 | Remapped | Perfect | NC_000001.10:g.(?_ 195255927)_(195580 212_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 195,255,927 | 195,580,212 |
| essv11638 | Submitted genomic | NC_000001.8:g.(?_1 91987584)_(1923118 69_?)dup | NCBI35 (hg17) | NC_000001.8 | Chr1 | 191,987,584 | 192,311,869 |