esv1838724
- 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:294,664
- 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: 707 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 707 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1838724 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 66,765,855 | 67,060,518 |
| esv1838724 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 67,232,573 | 67,527,235 |
| esv1838724 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 66,302,326 | 66,596,988 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4381858 | Remapped | Perfect | NC_000014.9:g.(?_6 6765855)_(67060518 _?)del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 66,765,855 | 67,060,518 |
| essv4381858 | Remapped | Perfect | NC_000014.8:g.(?_6 7232573)_(67527235 _?)del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 67,232,573 | 67,527,235 |
| essv4381858 | Submitted genomic | NC_000014.7:g.(?_6 6302326)_(66596988 _?)del | NCBI36 (hg18) | NC_000014.7 | Chr14 | 66,302,326 | 66,596,988 |