esv3691625
- Organism: Homo sapiens
- Study:estd220 (Pettigrew et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:216,571
- Publication(s):Pettigrew et al. 2015
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: 659 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 659 SVs from 64 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
esv3691625 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 39,162,506 | 39,162,506 | 39,264,493 | 39,379,076 |
esv3691625 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 39,184,056 | 39,184,056 | 39,286,043 | 39,400,626 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv16505932 | duplication | FR-31 | SNP array | SNP genotyping analysis | 42 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
essv16505932 | Remapped | Perfect | NC_000011.10:g.(39 162506_39162506)_( 39264493_39379076) dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 39,162,506 | 39,162,506 | 39,264,493 | 39,379,076 |
essv16505932 | Submitted genomic | NC_000011.9:g.(391 84056_39184056)_(3 9286043_39400626)d up169156 | GRCh37 (hg19) | NC_000011.9 | Chr11 | 39,184,056 | 39,184,056 | 39,286,043 | 39,400,626 |