esv2559667
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:originalFile=Yoruban_small_indel.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: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 9 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2559667 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 119,151,178 | 119,151,178 |
| esv2559667 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 118,870,025 | 118,870,025 |
| esv2559667 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 120,352,715 | 120,352,715 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5212411 | Remapped | Perfect | NC_000003.12:g.119 151178_119151179in s? | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 119,151,178 | 119,151,178 |
| essv5212411 | Remapped | Perfect | NC_000003.11:g.118 870025_118870026in s? | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 118,870,025 | 118,870,025 |
| essv5212411 | Submitted genomic | NC_000003.10:g.120 352715_120352716in s? | NCBI36 (hg18) | NC_000003.10 | Chr3 | 120,352,715 | 120,352,715 |