esv2757597
- 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:75,445
- 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: 323 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 323 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 11 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757597 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 41,754,975 | 41,830,419 |
| esv2757597 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 42,047,173 | 42,122,617 |
| esv2757597 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 39,834,465 | 39,909,909 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5698 | Remapped | Perfect | NC_000015.10:g.(41 754975_41754975)_( 41830419_41830419) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 41,754,975 | 41,754,975 | 41,830,419 | 41,830,419 |
| essv5698 | Remapped | Perfect | NC_000015.9:g.(420 47173_42047173)_(4 2122617_42122617)d el | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 42,047,173 | 42,047,173 | 42,122,617 | 42,122,617 |
| essv5698 | Submitted genomic | NC_000015.8:g.(398 34465_39834465)_(3 9909909_39909909)d el | NCBI35 (hg17) | NC_000015.8 | Chr15 | 39,834,465 | 39,834,465 | 39,909,909 | 39,909,909 |