esv996731
- 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:20,111
- 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: 964 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 964 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 538 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv996731 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 57,184,136 | 57,204,246 |
| esv996731 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 57,758,270 | 57,778,380 |
| esv996731 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 56,656,271 | 56,676,381 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586028 | Remapped | Perfect | NC_000013.11:g.(?_ 57184136)_(5720424 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 57,184,136 | 57,204,246 |
| essv3586028 | Remapped | Perfect | NC_000013.10:g.(?_ 57758270)_(5777838 0_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 57,758,270 | 57,778,380 |
| essv3586028 | Submitted genomic | NC_000013.9:g.(?_5 6656271)_(56676381 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 56,656,271 | 56,676,381 |