esv2490419
- 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:22,803
- 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: 334 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 334 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 132 SVs from 21 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 |
---|---|---|---|---|---|---|---|---|---|
esv2490419 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,893,463 | 1,916,265 |
esv2490419 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 1,914,693 | 1,937,495 |
esv2490419 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 1,871,269 | 1,894,071 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv5266279 | Remapped | Perfect | NC_000011.10:g.(18 93463_?)_(?_191626 5)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,893,463 | 1,916,265 |
essv5266279 | Remapped | Perfect | NC_000011.9:g.(191 4693_?)_(?_1937495 )del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 1,914,693 | 1,937,495 |
essv5266279 | Submitted genomic | NC_000011.8:g.(187 1269_?)_(?_1894071 )del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 1,871,269 | 1,894,071 |