esv274920
- Organism: Homo sapiens
- Study:estd176 (Banerjee et al. 2011)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,175
- Publication(s):Banerjee et al. 2011
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: 148 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 38 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv274920 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 45,685,162 | 45,687,729 | 45,688,194 | 45,688,336 |
| esv274920 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 45,977,360 | 45,979,927 | 45,980,392 | 45,980,534 |
| esv274920 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 43,764,652 | 43,767,219 | 43,767,684 | 43,767,826 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv2585494 | complex substitution | SNP array | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|
| essv2585494 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 45,685,162 | 45,687,729 | 45,688,194 | 45,688,336 |
| essv2585494 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 45,977,360 | 45,979,927 | 45,980,392 | 45,980,534 |
| essv2585494 | Submitted genomic | NCBI36 (hg18) | NC_000015.8 | Chr15 | 43,764,652 | 43,767,219 | 43,767,684 | 43,767,826 |