esv2757692
- 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:165,918
- 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: 681 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 681 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757692 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 24,156,918 | 24,322,835 |
| esv2757692 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 24,339,720 | 24,505,637 |
| esv2757692 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000019.8 | Chr19 | 24,131,560 | 24,297,477 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv7645 | Remapped | Perfect | NC_000019.10:g.(24 156918_24157700)_( 24279607_24322835) dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 24,156,918 | 24,157,700 | 24,279,607 | 24,322,835 |
| essv7645 | Remapped | Perfect | NC_000019.9:g.(243 39720_24340502)_(2 4462409_24505637)d up | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 24,339,720 | 24,340,502 | 24,462,409 | 24,505,637 |
| essv7645 | Submitted genomic | NC_000019.8:g.(241 31560_24132342)_(2 4254249_24297477)d up | NCBI35 (hg17) | NC_000019.8 | Chr19 | 24,131,560 | 24,132,342 | 24,254,249 | 24,297,477 |