esv3692851
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:49,834
- Publication(s):Palta et al. 2015
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: 350 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 350 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 120 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3692851 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 167,107,984 | 167,157,817 |
| esv3692851 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 168,029,135 | 168,078,968 |
| esv3692851 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 168,265,710 | 168,315,543 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16508909 | Remapped | Perfect | NC_000004.12:g.(?_ 167107984)_(167157 817_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 167,107,984 | 167,157,817 |
| essv16508909 | Remapped | Perfect | NC_000004.11:g.(?_ 168029135)_(168078 968_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 168,029,135 | 168,078,968 |
| essv16508909 | Submitted genomic | NC_000004.10:g.(?_ 168265710)_(168315 543_?)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 168,265,710 | 168,315,543 |