esv1826972
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:223,129
- Publication(s):Pinto et al. 2011
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: 777 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 777 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 279 SVs from 17 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 |
---|---|---|---|---|---|---|---|---|---|
esv1826972 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 107,806,947 | 108,030,075 |
esv1826972 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 109,566,705 | 109,789,833 |
esv1826972 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 109,556,695 | 109,779,823 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv4367818 | Remapped | Perfect | NC_000010.11:g.(?_ 107806947)_(108030 075_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 107,806,947 | 108,030,075 |
essv4367818 | Remapped | Perfect | NC_000010.10:g.(?_ 109566705)_(109789 833_?)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 109,566,705 | 109,789,833 |
essv4367818 | Submitted genomic | NC_000010.9:g.(?_1 09556695)_(1097798 23_?)del | NCBI36 (hg18) | NC_000010.9 | Chr10 | 109,556,695 | 109,779,823 |