esv2761170
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,634
- Publication(s):Vogler 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: 277 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 277 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 142 SVs from 10 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
esv2761170 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 18,176,663 | 18,179,296 |
esv2761170 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 18,034,172 | 18,036,805 |
esv2761170 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 18,078,452 | 18,081,085 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv7016514 | Remapped | Perfect | NC_000008.11:g.(?_ 18176663)_(1817929 6_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 18,176,663 | 18,179,296 |
essv7016515 | Remapped | Perfect | NC_000008.11:g.(?_ 18176663)_(1817929 6_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 18,176,663 | 18,179,296 |
essv7016516 | Remapped | Perfect | NC_000008.11:g.(?_ 18177517)_(1817929 6_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 18,177,517 | 18,179,296 |
essv7016514 | Remapped | Perfect | NC_000008.10:g.(?_ 18034172)_(1803680 5_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 18,034,172 | 18,036,805 |
essv7016515 | Remapped | Perfect | NC_000008.10:g.(?_ 18034172)_(1803680 5_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 18,034,172 | 18,036,805 |
essv7016516 | Remapped | Perfect | NC_000008.10:g.(?_ 18035026)_(1803680 5_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 18,035,026 | 18,036,805 |
essv7016514 | Submitted genomic | NC_000008.9:g.(?_1 8078452)_(18081085 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 18,078,452 | 18,081,085 | ||
essv7016515 | Submitted genomic | NC_000008.9:g.(?_1 8078452)_(18081085 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 18,078,452 | 18,081,085 | ||
essv7016516 | Submitted genomic | NC_000008.9:g.(?_1 8079306)_(18081085 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 18,079,306 | 18,081,085 |