esv1001271
- 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:10,030
- 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: 262 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 262 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 14 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 |
---|---|---|---|---|---|---|---|---|---|
esv1001271 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 42,006,616 | 42,016,645 |
esv1001271 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 39,586,580 | 39,596,609 |
esv1001271 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 37,840,578 | 37,850,607 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv3564828 | Remapped | Perfect | NC_000018.10:g.(42 006616_?)_(?_42016 645)ins12218 | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,006,616 | 42,016,645 |
essv3564828 | Remapped | Perfect | NC_000018.9:g.(395 86580_?)_(?_395966 09)ins12218 | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,586,580 | 39,596,609 |
essv3564828 | Submitted genomic | NC_000018.8:g.(378 40578_?)_(?_378506 07)ins12218 | NCBI36 (hg18) | NC_000018.8 | Chr18 | 37,840,578 | 37,850,607 |