esv2757398
- Organism: Homo sapiens
- Study:estd1 (Redon et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:200,577
- Publication(s):Redon et al. 2006
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: 394 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 394 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 26 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757398 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 75,776,288 | 75,976,864 |
| esv2757398 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 77,536,046 | 77,736,622 |
| esv2757398 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 77,206,052 | 77,406,628 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv19319 | Remapped | Perfect | NC_000010.11:g.(75 776288_75788418)_( 75940477_75976864) dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 75,776,288 | 75,788,418 | 75,940,477 | 75,976,864 |
| essv19319 | Remapped | Perfect | NC_000010.10:g.(77 536046_77548176)_( 77700235_77736622) dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 77,536,046 | 77,548,176 | 77,700,235 | 77,736,622 |
| essv19319 | Submitted genomic | NC_000010.8:g.(772 06052_77218182)_(7 7370241_77406628)d up | NCBI35 (hg17) | NC_000010.8 | Chr10 | 77,206,052 | 77,218,182 | 77,370,241 | 77,406,628 |