esv1011203
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:22,502
- Publication(s):Pang et al. 2010
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: 335 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 65 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 335 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 155 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 | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|
| esv1011203 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 141,403,605 | - | 141,426,106 |
| esv1011203 | Remapped | Pass | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187574.1 | Chr8|NT_18 7574.1 | 70,209 | 82,401 | - |
| esv1011203 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 142,413,705 | - | 142,436,206 |
| esv1011203 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 142,482,887 | - | 142,505,388 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|
| essv3565632 | Remapped | Pass | NT_187574.1:g.(702 09_?)_(82401_?)ins 12814 | GRCh38.p12 | Second Pass | NT_187574.1 | Chr8|NT_18 7574.1 | 70,209 | 82,401 | - |
| essv3565632 | Remapped | Perfect | NC_000008.11:g.(14 1403605_?)_(?_1414 26106)ins12814 | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 141,403,605 | - | 141,426,106 |
| essv3565632 | Remapped | Perfect | NC_000008.10:g.(14 2413705_?)_(?_1424 36206)ins12814 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 142,413,705 | - | 142,436,206 |
| essv3565632 | Submitted genomic | NC_000008.9:g.(142 482887_?)_(?_14250 5388)ins12814 | NCBI36 (hg18) | NC_000008.9 | Chr8 | 142,482,887 | - | 142,505,388 |