esv2760965
- 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:134,275
- 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: 705 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 710 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 275 SVs from 23 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 |
---|---|---|---|---|---|---|---|---|---|
esv2760965 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 238,486,457 | 238,620,731 |
esv2760965 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 238,649,757 | 238,784,031 |
esv2760965 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 236,716,380 | 236,850,654 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv7005933 | Remapped | Perfect | NC_000001.11:g.(?_ 238486457)_(238620 731_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 238,486,457 | 238,620,731 |
essv7005944 | Remapped | Perfect | NC_000001.11:g.(?_ 238491255)_(238615 306_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 238,491,255 | 238,615,306 |
essv7005933 | Remapped | Perfect | NC_000001.10:g.(?_ 238649757)_(238784 031_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 238,649,757 | 238,784,031 |
essv7005944 | Remapped | Perfect | NC_000001.10:g.(?_ 238654555)_(238778 606_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 238,654,555 | 238,778,606 |
essv7005933 | Submitted genomic | NC_000001.9:g.(?_2 36716380)_(2368506 54_?)dup | NCBI36 (hg18) | NC_000001.9 | Chr1 | 236,716,380 | 236,850,654 | ||
essv7005944 | Submitted genomic | NC_000001.9:g.(?_2 36721178)_(2368452 29_?)dup | NCBI36 (hg18) | NC_000001.9 | Chr1 | 236,721,178 | 236,845,229 |