esv999516
- 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:32,799
- 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: 255 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 63 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 255 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 30 SVs from 13 studies. See in: genome view
Overlapping variant regions from other studies: 65 SVs from 17 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 |
---|---|---|---|---|---|---|---|---|---|
esv999516 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 155,950,432 | 155,970,576 |
esv999516 | Remapped | Pass | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NW_003315914.1 | Chr4|NW_00 3315914.1 | 115,050 | 147,848 |
esv999516 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 156,871,584 | 156,891,728 |
esv999516 | Remapped | Pass | GRCh37.p13 | PATCHES | Second Pass | NW_003315914.1 | Chr4|NW_00 3315914.1 | 115,050 | 147,848 |
esv999516 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 157,091,034 | 157,111,178 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv3563755 | Remapped | Pass | NW_003315914.1:g.( 115050_?)_(?_14784 8)ins15021 | GRCh38.p12 | Second Pass | NW_003315914.1 | Chr4|NW_00 3315914.1 | 115,050 | 147,848 |
essv3563755 | Remapped | Perfect | NC_000004.12:g.(15 5950432_?)_(?_1559 70576)ins15021 | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 155,950,432 | 155,970,576 |
essv3563755 | Remapped | Pass | NW_003315914.1:g.( 115050_?)_(?_14784 8)ins15021 | GRCh37.p13 | Second Pass | NW_003315914.1 | Chr4|NW_00 3315914.1 | 115,050 | 147,848 |
essv3563755 | Remapped | Perfect | NC_000004.11:g.(15 6871584_?)_(?_1568 91728)ins15021 | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 156,871,584 | 156,891,728 |
essv3563755 | Submitted genomic | NC_000004.10:g.(15 7091034_?)_(?_1571 11178)ins15021 | NCBI36 (hg18) | NC_000004.10 | Chr4 | 157,091,034 | 157,111,178 |