esv1005872
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:26,586
- 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: 533 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 93 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1005872 | Remapped | Good | GRCh38.p12 | Primary Assembly | Second Pass | NC_000009.12 | Chr9 | 66,181,962 | 66,208,547 |
| esv1005872 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 70,707,924 | 70,735,468 |
| esv1005872 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 69,947,744 | 69,975,288 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586554 | Remapped | Good | NC_000009.12:g.(?_ 66181962)_(6620854 7_?)dup | GRCh38.p12 | Second Pass | NC_000009.12 | Chr9 | 66,181,962 | 66,208,547 |
| essv3586554 | Remapped | Perfect | NC_000009.11:g.(?_ 70707924)_(7073546 8_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 70,707,924 | 70,735,468 |
| essv3586554 | Submitted genomic | NC_000009.10:g.(?_ 69947744)_(6997528 8_?)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 69,947,744 | 69,975,288 |