esv2756789
- 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:268,779
- 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: 622 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 622 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 46 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2756789 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 89,739,590 | 90,008,368 |
| esv2756789 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 88,994,589 | 89,263,367 |
| esv2756789 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 88,800,734 | 89,069,512 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv4543 | Remapped | Perfect | NC_000023.11:g.(89 739590_89773375)_( 89901240_90008368) dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 89,739,590 | 89,773,375 | 89,901,240 | 90,008,368 |
| essv4543 | Remapped | Perfect | NC_000023.10:g.(88 994589_89028374)_( 89156239_89263367) dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 88,994,589 | 89,028,374 | 89,156,239 | 89,263,367 |
| essv4543 | Submitted genomic | NC_000023.8:g.(888 00734_88834519)_(8 8962384_89069512)d up | NCBI35 (hg17) | NC_000023.8 | ChrX | 88,800,734 | 88,834,519 | 88,962,384 | 89,069,512 |