esv2422464
- Organism: Homo sapiens
- Study:estd196 (Simon-Sanchez et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:26,588
- Publication(s):Simon-Sanchez et al. 2006
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: 191 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 190 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 12 SVs from 4 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 |
---|---|---|---|---|---|---|---|---|---|
esv2422464 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 57,419,367 | 57,445,954 |
esv2422464 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 55,496,728 | 55,523,315 |
esv2422464 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000017.9 | Chr17 | 52,851,727 | 52,878,314 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv5161506 | Remapped | Perfect | NC_000017.11:g.(?_ 57419367)_(5744595 4_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 57,419,367 | 57,445,954 |
essv5161506 | Remapped | Perfect | NC_000017.10:g.(?_ 55496728)_(5552331 5_?)dup | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 55,496,728 | 55,523,315 |
essv5161506 | Submitted genomic | NC_000017.9:g.(?_5 2851727)_(52878314 _?)dup | NCBI35 (hg17) | NC_000017.9 | Chr17 | 52,851,727 | 52,878,314 |