esv2757473
- 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:179,678
- 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: 686 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 686 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 38 SVs from 7 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 |
---|---|---|---|---|---|---|---|---|---|
esv2757473 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 103,165,062 | 103,344,739 |
esv2757473 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 103,035,791 | 103,215,467 |
esv2757473 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 102,541,001 | 102,720,677 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv5763 | Remapped | Good | NC_000011.10:g.(10 3165062_103165062) _(103344739_103344 739)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 103,165,062 | 103,165,062 | 103,344,739 | 103,344,739 |
essv5763 | Remapped | Perfect | NC_000011.9:g.(103 035791_103067460)_ (103215467_1032154 67)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 103,035,791 | 103,067,460 | 103,215,467 | 103,215,467 |
essv5763 | Submitted genomic | NC_000011.8:g.(102 541001_102572670)_ (102720677_1027206 77)del | NCBI35 (hg17) | NC_000011.8 | Chr11 | 102,541,001 | 102,572,670 | 102,720,677 | 102,720,677 |