esv2569789
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,575
- Description:originalFile=Yoruban_large_indels_8.4x.gff
- Publication(s):McKernan et al. 2009
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: 235 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 235 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 77 SVs from 18 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
esv2569789 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 77,617,833 | 77,619,407 |
esv2569789 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 77,910,175 | 77,911,749 |
esv2569789 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 75,697,230 | 75,698,804 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv5266481 | Remapped | Perfect | NC_000015.10:g.(77 617833_?)_(?_77619 407)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 77,617,833 | 77,619,407 |
essv5266481 | Remapped | Perfect | NC_000015.9:g.(779 10175_?)_(?_779117 49)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 77,910,175 | 77,911,749 |
essv5266481 | Submitted genomic | NC_000015.8:g.(756 97230_?)_(?_756988 04)del | NCBI36 (hg18) | NC_000015.8 | Chr15 | 75,697,230 | 75,698,804 |