esv3693446
- 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:47,917
- 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: 236 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 83 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3693446 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 182,920,870 | 182,968,786 |
| esv3693446 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 183,785,598 | 183,833,514 |
| esv3693446 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 183,493,843 | 183,541,759 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16507352 | Remapped | Perfect | NC_000002.12:g.(?_ 182920870)_(182968 786_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 182,920,870 | 182,968,786 |
| essv16507352 | Remapped | Perfect | NC_000002.11:g.(?_ 183785598)_(183833 514_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 183,785,598 | 183,833,514 |
| essv16507352 | Submitted genomic | NC_000002.10:g.(?_ 183493843)_(183541 759_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,493,843 | 183,541,759 |