esv2764111
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:137,108
- 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: 671 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 671 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 235 SVs from 19 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 |
---|---|---|---|---|---|---|---|---|---|
esv2764111 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 137,831,925 | 137,969,032 |
esv2764111 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 138,844,168 | 138,981,275 |
esv2764111 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 138,913,350 | 139,050,457 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv6993464 | Remapped | Perfect | NC_000008.11:g.(?_ 137831925)_(137948 588_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 137,831,925 | 137,948,588 |
essv6993465 | Remapped | Perfect | NC_000008.11:g.(?_ 137870903)_(137969 032_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 137,870,903 | 137,969,032 |
essv6993464 | Remapped | Perfect | NC_000008.10:g.(?_ 138844168)_(138960 831_?)dup | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 138,844,168 | 138,960,831 |
essv6993465 | Remapped | Perfect | NC_000008.10:g.(?_ 138883146)_(138981 275_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 138,883,146 | 138,981,275 |
essv6993464 | Submitted genomic | NC_000008.9:g.(?_1 38913350)_(1390300 13_?)dup | NCBI36 (hg18) | NC_000008.9 | Chr8 | 138,913,350 | 139,030,013 | ||
essv6993465 | Submitted genomic | NC_000008.9:g.(?_1 38952328)_(1390504 57_?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 138,952,328 | 139,050,457 |