esv1844081
- 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:421,075
- 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: 4245 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 4278 SVs from 103 studies. See in: genome view
Overlapping variant regions from other studies: 2668 SVs from 32 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1844081 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 32,478,126 | 32,899,200 |
| esv1844081 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 32,489,447 | 32,910,521 |
| esv1844081 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 32,396,948 | 32,818,022 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4396614 | Remapped | Perfect | NC_000016.10:g.(?_ 32478126)_(3289920 0_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,478,126 | 32,899,200 |
| essv4396614 | Remapped | Perfect | NC_000016.9:g.(?_3 2489447)_(32910521 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 32,489,447 | 32,910,521 |
| essv4396614 | Submitted genomic | NC_000016.8:g.(?_3 2396948)_(32818022 _?)dup | NCBI36 (hg18) | NC_000016.8 | Chr16 | 32,396,948 | 32,818,022 |