esv1826642
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:214,948
- Publication(s):Pinto 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: 714 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 714 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 265 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1826642 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 34,919,148 | 35,134,095 |
| esv1826642 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 35,493,285 | 35,708,232 |
| esv1826642 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 34,391,285 | 34,606,232 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4404399 | Remapped | Perfect | NC_000013.11:g.(?_ 34919148)_(3513409 5_?)dup | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 34,919,148 | 35,134,095 |
| essv4404399 | Remapped | Perfect | NC_000013.10:g.(?_ 35493285)_(3570823 2_?)dup | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 35,493,285 | 35,708,232 |
| essv4404399 | Submitted genomic | NC_000013.9:g.(?_3 4391285)_(34606232 _?)dup | NCBI36 (hg18) | NC_000013.9 | Chr13 | 34,391,285 | 34,606,232 |