esv1010773
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:18,930
- Publication(s):Pang 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: 29 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 433 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 265 SVs from 24 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1010773 | Remapped | Pass | GRCh38.p12 | PATCHES | First Pass | NW_015495298.1 | Chr1|NW_01 5495298.1 | 215,876 | 234,805 |
| esv1010773 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 13,102,999 | 13,124,417 |
| esv1010773 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 13,025,586 | 13,047,004 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586120 | Remapped | Pass | NW_015495298.1:g.( ?_215876)_(234805_ ?)dup | GRCh38.p12 | First Pass | NW_015495298.1 | Chr1|NW_01 5495298.1 | 215,876 | 234,805 |
| essv3586120 | Remapped | Perfect | NC_000001.10:g.(?_ 13102999)_(1312441 7_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 13,102,999 | 13,124,417 |
| essv3586120 | Submitted genomic | NC_000001.9:g.(?_1 3025586)_(13047004 _?)dup | NCBI36 (hg18) | NC_000001.9 | Chr1 | 13,025,586 | 13,047,004 |