esv29995
- 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:14,174
- 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: 1346 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1346 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 856 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29995 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 32,643,036 | 32,657,209 |
| esv29995 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 32,610,813 | 32,624,986 |
| esv29995 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 32,718,791 | 32,732,964 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84234 | Remapped | Perfect | NC_000006.12:g.(?_ 32643036)_(3265720 9_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 32,643,036 | 32,657,209 |
| essv84234 | Remapped | Perfect | NC_000006.11:g.(?_ 32610813)_(3262498 6_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 32,610,813 | 32,624,986 |
| essv84234 | Submitted genomic | NC_000006.10:g.(?_ 32718791)_(3273296 4_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 32,718,791 | 32,732,964 |