esv2761903
- Organism: Homo sapiens
- Study:estd203 (Vogler 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:57,867
- Publication(s):Vogler 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: 191 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 191 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 34 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2761903 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 19,734,658 | 19,792,524 |
| esv2761903 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 19,745,980 | 19,803,846 |
| esv2761903 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 19,653,481 | 19,711,347 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7000592 | copy number gain | SW_1026 | SNP array | SNP genotyping analysis | 48 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv7000592 | Remapped | Perfect | NC_000016.10:g.(?_ 19734658)_(1979252 4_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 19,734,658 | 19,792,524 |
| essv7000592 | Remapped | Perfect | NC_000016.9:g.(?_1 9745980)_(19803846 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 19,745,980 | 19,803,846 |
| essv7000592 | Submitted genomic | NC_000016.8:g.(?_1 9653481)_(19711347 _?)dup | NCBI36 (hg18) | NC_000016.8 | Chr16 | 19,653,481 | 19,711,347 |