esv3693442
- 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:20,355
- 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 29 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 95 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3693442 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 176,314,043 | 176,334,397 |
| esv3693442 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 177,178,771 | 177,199,125 |
| esv3693442 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 176,887,017 | 176,907,371 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16507472 | Remapped | Perfect | NC_000002.12:g.(?_ 176314043)_(176334 397_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 176,314,043 | 176,334,397 |
| essv16507472 | Remapped | Perfect | NC_000002.11:g.(?_ 177178771)_(177199 125_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 177,178,771 | 177,199,125 |
| essv16507472 | Submitted genomic | NC_000002.10:g.(?_ 176887017)_(176907 371_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 176,887,017 | 176,907,371 |