esv2764075
- 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:71,857
- 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: 505 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 505 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 18 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 |
---|---|---|---|---|---|---|---|---|---|
esv2764075 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 15,715,932 | 15,787,788 |
esv2764075 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 15,573,441 | 15,645,297 |
esv2764075 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 15,617,812 | 15,689,668 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv6992754 | Remapped | Perfect | NC_000008.11:g.(?_ 15715932)_(1578778 8_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 15,715,932 | 15,787,788 |
essv6992755 | Remapped | Perfect | NC_000008.11:g.(?_ 15743653)_(1576534 9_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 15,743,653 | 15,765,349 |
essv6992757 | Remapped | Perfect | NC_000008.11:g.(?_ 15743907)_(1576534 9_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 15,743,907 | 15,765,349 |
essv6992754 | Remapped | Perfect | NC_000008.10:g.(?_ 15573441)_(1564529 7_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 15,573,441 | 15,645,297 |
essv6992755 | Remapped | Perfect | NC_000008.10:g.(?_ 15601162)_(1562285 8_?)dup | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 15,601,162 | 15,622,858 |
essv6992757 | Remapped | Perfect | NC_000008.10:g.(?_ 15601416)_(1562285 8_?)dup | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 15,601,416 | 15,622,858 |
essv6992754 | Submitted genomic | NC_000008.9:g.(?_1 5617812)_(15689668 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 15,617,812 | 15,689,668 | ||
essv6992755 | Submitted genomic | NC_000008.9:g.(?_1 5645533)_(15667229 _?)dup | NCBI36 (hg18) | NC_000008.9 | Chr8 | 15,645,533 | 15,667,229 | ||
essv6992757 | Submitted genomic | NC_000008.9:g.(?_1 5645787)_(15667229 _?)dup | NCBI36 (hg18) | NC_000008.9 | Chr8 | 15,645,787 | 15,667,229 |