esv2761844
- 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:4,713
- 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: 109 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 109 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 21 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2761844 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 73,825,236 | 73,829,948 |
| esv2761844 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 74,291,939 | 74,296,651 |
| esv2761844 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 73,361,692 | 73,366,404 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv6998677 | copy number loss | SW_0593 | SNP array | SNP genotyping analysis | 23 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv6998677 | Remapped | Perfect | NC_000014.9:g.(?_7 3825236)_(73829948 _?)del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 73,825,236 | 73,829,948 |
| essv6998677 | Remapped | Perfect | NC_000014.8:g.(?_7 4291939)_(74296651 _?)del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 74,291,939 | 74,296,651 |
| essv6998677 | Submitted genomic | NC_000014.7:g.(?_7 3361692)_(73366404 _?)del | NCBI36 (hg18) | NC_000014.7 | Chr14 | 73,361,692 | 73,366,404 |