esv30005
- 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:81,041
- 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: 786 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 786 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 395 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv30005 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 136,481,974 | 136,563,014 |
| esv30005 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 139,376,426 | 139,457,466 |
| esv30005 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 138,496,247 | 138,577,287 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84244 | Remapped | Perfect | NC_000009.12:g.(?_ 136481974)_(136563 014_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 136,481,974 | 136,563,014 |
| essv84244 | Remapped | Perfect | NC_000009.11:g.(?_ 139376426)_(139457 466_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 139,376,426 | 139,457,466 |
| essv84244 | Submitted genomic | NC_000009.10:g.(?_ 138496247)_(138577 287_?)del | NCBI36 (hg18) | NC_000009.10 | Chr9 | 138,496,247 | 138,577,287 |