esv2757468
- Organism: Homo sapiens
- Study:estd1 (Redon et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:129,491
- 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: 467 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 467 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 20 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757468 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 97,743,840 | 97,873,330 |
| esv2757468 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 97,614,840 | 97,744,330 |
| esv2757468 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 97,120,050 | 97,249,540 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv997 | Remapped | Perfect | NC_000011.10:g.(97 743840_97752375)_( 97817067_97873330) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 97,743,840 | 97,752,375 | 97,817,067 | 97,873,330 |
| essv997 | Remapped | Perfect | NC_000011.9:g.(976 14840_97623375)_(9 7688067_97744330)d el | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 97,614,840 | 97,623,375 | 97,688,067 | 97,744,330 |
| essv997 | Submitted genomic | NC_000011.8:g.(971 20050_97128585)_(9 7193277_97249540)d el | NCBI35 (hg17) | NC_000011.8 | Chr11 | 97,120,050 | 97,128,585 | 97,193,277 | 97,249,540 |