esv29993
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:125,570
- Publication(s):Levy et al. 2007
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: 329 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 329 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29993 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 63,971,170 | 64,096,739 |
| esv29993 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 63,738,642 | 63,864,211 |
| esv29993 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 63,495,218 | 63,620,787 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84232 | Remapped | Perfect | NC_000011.10:g.(?_ 63971170)_(6409673 9_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 63,971,170 | 64,096,739 |
| essv84232 | Remapped | Perfect | NC_000011.9:g.(?_6 3738642)_(63864211 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 63,738,642 | 63,864,211 |
| essv84232 | Submitted genomic | NC_000011.8:g.(?_6 3495218)_(63620787 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 63,495,218 | 63,620,787 |