esv1825714
- 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:337,025
- 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: 538 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 1599 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 581 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1825714 | Remapped | Pass | GRCh38.p12 | Primary Assembly | Second Pass | NC_000022.11 | Chr22 | 12,285,218 | 12,622,242 |
| esv1825714 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 68,397,586 | 68,747,506 |
| esv1825714 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 67,887,406 | 68,137,326 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4376775 | Remapped | Pass | NC_000022.11:g.(?_ 12285218)_(1262224 2_?)dup | GRCh38.p12 | Second Pass | NC_000022.11 | Chr22 | 12,285,218 | 12,622,242 |
| essv4376775 | Remapped | Pass | NC_000009.11:g.(?_ 68397586)_(6874750 6_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 68,397,586 | 68,747,506 |
| essv4376775 | Submitted genomic | NC_000009.10:g.(?_ 67887406)_(6813732 6_?)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 67,887,406 | 68,137,326 |