esv2757186
- 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:94,258
- 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: 381 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 381 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 20 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757186 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 92,867,699 | 92,961,956 |
| esv2757186 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 93,577,417 | 93,671,674 |
| esv2757186 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 93,634,138 | 93,728,395 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv1000 | Remapped | Perfect | NC_000006.12:g.(92 867699_92878969)_( 92909209_92961956) dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 92,867,699 | 92,878,969 | 92,909,209 | 92,961,956 |
| essv1000 | Remapped | Perfect | NC_000006.11:g.(93 577417_93588687)_( 93618927_93671674) dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 93,577,417 | 93,588,687 | 93,618,927 | 93,671,674 |
| essv1000 | Submitted genomic | NC_000006.9:g.(936 34138_93645408)_(9 3675648_93728395)d up | NCBI35 (hg17) | NC_000006.9 | Chr6 | 93,634,138 | 93,645,408 | 93,675,648 | 93,728,395 |