esv1008241
- 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:26,391
- 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: 153 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 32 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 153 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 45 SVs from 15 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 |
---|---|---|---|---|---|---|---|---|---|
esv1008241 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 112,150,996 | 112,167,901 |
esv1008241 | Remapped | Pass | GRCh38.p12 | PATCHES | Second Pass | NW_019805492.1 | Chr3|NW_01 9805492.1 | 34,286 | 60,676 |
esv1008241 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 111,869,843 | 111,886,748 |
esv1008241 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 113,352,533 | 113,369,438 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv3563639 | Remapped | Pass | NW_019805492.1:g.( 34286_?)_(?_60676) ins14324 | GRCh38.p12 | Second Pass | NW_019805492.1 | Chr3|NW_01 9805492.1 | 34,286 | 60,676 |
essv3563639 | Remapped | Perfect | NC_000003.12:g.(11 2150996_?)_(?_1121 67901)ins14324 | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 112,150,996 | 112,167,901 |
essv3563639 | Remapped | Perfect | NC_000003.11:g.(11 1869843_?)_(?_1118 86748)ins14324 | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 111,869,843 | 111,886,748 |
essv3563639 | Submitted genomic | NC_000003.10:g.(11 3352533_?)_(?_1133 69438)ins14324 | NCBI36 (hg18) | NC_000003.10 | Chr3 | 113,352,533 | 113,369,438 |