esv3692830
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:43,747
- Publication(s):Palta et al. 2015
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: 297 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 297 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3692830 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 97,704,346 | 97,748,092 |
| esv3692830 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 98,625,497 | 98,669,243 |
| esv3692830 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 98,844,520 | 98,888,266 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16507260 | Remapped | Perfect | NC_000004.12:g.(?_ 97704346)_(9774809 2_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 97,704,346 | 97,748,092 |
| essv16507260 | Remapped | Perfect | NC_000004.11:g.(?_ 98625497)_(9866924 3_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 98,625,497 | 98,669,243 |
| essv16507260 | Submitted genomic | NC_000004.10:g.(?_ 98844520)_(9888826 6_?)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 98,844,520 | 98,888,266 |