esv994373
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:127,891
- Publication(s):Pang et al. 2010
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: 848 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1372 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 925 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv994373 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 61,520,009 | 61,647,899 |
| esv994373 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 44,727,847 | 44,855,737 |
| esv994373 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 44,667,843 | 44,795,733 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586004 | Remapped | Perfect | NC_000009.12:g.(?_ 61520009)_(6164789 9_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 61,520,009 | 61,647,899 |
| essv3586004 | Remapped | Perfect | NC_000009.11:g.(?_ 44727847)_(4485573 7_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 44,727,847 | 44,855,737 |
| essv3586004 | Submitted genomic | NC_000009.10:g.(?_ 44667843)_(4479573 3_?)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 44,667,843 | 44,795,733 |