esv2280101
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,503
- Publication(s):Bentley et al. 2008
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: 284 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 284 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 20 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
esv2280101 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 80,033,824 | 80,033,893 | 80,043,226 | 80,043,326 |
esv2280101 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 81,793,580 | 81,793,649 | 81,802,982 | 81,803,082 |
esv2280101 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 81,783,560 | 81,783,629 | 81,792,962 | 81,793,062 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv4559726 | Remapped | Perfect | NC_000010.11:g.(80 033824_80033893)_( 80043226_80043326) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 80,033,824 | 80,033,893 | 80,043,226 | 80,043,326 |
essv4559726 | Remapped | Perfect | NC_000010.10:g.(81 793580_81793649)_( 81802982_81803082) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 81,793,580 | 81,793,649 | 81,802,982 | 81,803,082 |
essv4559726 | Submitted genomic | NC_000010.9:g.(817 83560_81783629)_(8 1792962_81793062)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 81,783,560 | 81,783,629 | 81,792,962 | 81,793,062 |