esv1825530
- 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:1,388,454
- 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: 4354 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 4354 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 1215 SVs from 26 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
esv1825530 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 178,489,485 | 179,877,938 |
esv1825530 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 179,410,639 | 180,799,091 |
esv1825530 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 179,647,633 | 181,036,085 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv4375151 | Remapped | Perfect | NC_000004.12:g.(?_ 178489485)_(179877 938_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 178,489,485 | 179,877,938 |
essv4375151 | Remapped | Perfect | NC_000004.11:g.(?_ 179410639)_(180799 091_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 179,410,639 | 180,799,091 |
essv4375151 | Submitted genomic | NC_000004.10:g.(?_ 179647633)_(181036 085_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 179,647,633 | 181,036,085 |