esv1830182
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:186,886
- Publication(s):Pinto et al. 2011
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: 885 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 885 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 281 SVs from 29 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
esv1830182 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 167,887,011 | 167,888,672 | 168,070,673 | 168,073,896 |
esv1830182 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 168,808,162 | 168,809,823 | 168,991,824 | 168,995,047 |
esv1830182 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 169,044,737 | 169,046,398 | 169,228,399 | 169,231,622 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
essv4421219 | Remapped | Perfect | NC_000004.12:g.(16 7887011_167888672) _(168070673_168073 896)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 167,887,011 | 167,888,672 | 168,070,673 | 168,073,896 |
essv4421219 | Remapped | Perfect | NC_000004.11:g.(16 8808162_168809823) _(168991824_168995 047)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 168,808,162 | 168,809,823 | 168,991,824 | 168,995,047 |
essv4421219 | Submitted genomic | NC_000004.10:g.(16 9044737_169046398) _(169228399_169231 622)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 169,044,737 | 169,046,398 | 169,228,399 | 169,231,622 |