esv2722215
- Organism: Homo sapiens
- Study:estd201 (Wong et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:80,378
- Publication(s):Wong et al. 2013
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: 1340 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1340 SVs from 84 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 |
---|---|---|---|---|---|---|---|---|---|
esv2722215 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 14,935,200 | 15,015,577 |
esv2722215 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 14,915,846 | 14,996,223 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv6882951 | Remapped | Perfect | NC_000020.11:g.(14 935200_?)_(?_15015 577)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 14,935,200 | 15,015,577 |
essv6688979 | Remapped | Perfect | NC_000020.11:g.(15 000338_?)_(?_15000 650)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 15,000,338 | 15,000,650 |
essv6832157 | Remapped | Perfect | NC_000020.11:g.(15 000345_?)_(?_15000 653)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 15,000,345 | 15,000,653 |
essv6882951 | Submitted genomic | NC_000020.10:g.(14 915846_?)_(?_14996 223)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 14,915,846 | 14,996,223 | ||
essv6688979 | Submitted genomic | NC_000020.10:g.(14 980984_?)_(?_14981 296)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 14,980,984 | 14,981,296 | ||
essv6832157 | Submitted genomic | NC_000020.10:g.(14 980991_?)_(?_14981 299)del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 14,980,991 | 14,981,299 |