esv994553
- 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:11,613
- 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: 650 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 650 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 424 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| esv994553 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 2,641,028 | - | 2,652,640 |
| esv994553 | Remapped | Pass | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187515.1 | Chr1|NT_18 7515.1 | 191,813 | 200,620 | - |
| esv994553 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 2,572,467 | - | 2,584,079 |
| esv994553 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 2,562,327 | - | 2,573,939 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|
| essv3565426 | Remapped | Pass | NT_187515.1:g.(191 813_?)_(200620_?)i ns13906 | GRCh38.p12 | Second Pass | NT_187515.1 | Chr1|NT_18 7515.1 | 191,813 | 200,620 | - |
| essv3565426 | Remapped | Perfect | NC_000001.11:g.(26 41028_?)_(?_265264 0)ins13906 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 2,641,028 | - | 2,652,640 |
| essv3565426 | Remapped | Perfect | NC_000001.10:g.(25 72467_?)_(?_258407 9)ins13906 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 2,572,467 | - | 2,584,079 |
| essv3565426 | Submitted genomic | NC_000001.9:g.(256 2327_?)_(?_2573939 )ins13906 | NCBI36 (hg18) | NC_000001.9 | Chr1 | 2,562,327 | - | 2,573,939 |