esv29991
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:11,625
- Publication(s):Levy et al. 2007
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: 570 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 570 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 261 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29991 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 180,991,312 | 181,002,936 |
| esv29991 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 180,418,312 | 180,429,936 |
| esv29991 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 180,350,918 | 180,362,542 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84230 | Remapped | Perfect | NC_000005.10:g.(?_ 180991312)_(181002 936_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 180,991,312 | 181,002,936 |
| essv84230 | Remapped | Perfect | NC_000005.9:g.(?_1 80418312)_(1804299 36_?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 180,418,312 | 180,429,936 |
| essv84230 | Submitted genomic | NC_000005.8:g.(?_1 80350918)_(1803625 42_?)dup | NCBI36 (hg18) | NC_000005.8 | Chr5 | 180,350,918 | 180,362,542 |