nsv817671
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:63,874
- Publication(s):Wang 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: 1975 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 1975 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 118 SVs from 11 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 |
---|---|---|---|---|---|---|---|---|---|
nsv817671 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 24,223,582 | 24,287,455 |
nsv817671 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 24,468,729 | 24,532,602 |
nsv817671 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 22,019,822 | 22,083,695 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1416873 | Remapped | Perfect | NC_000015.10:g.(?_ 24223582)_(2428745 5_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 24,223,582 | 24,287,455 |
nssv1416873 | Remapped | Perfect | NC_000015.9:g.(?_2 4468729)_(24532602 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 24,468,729 | 24,532,602 |
nssv1416873 | Submitted genomic | NC_000015.8:g.(?_2 2019822)_(22083695 _?)del | NCBI35 (hg17) | NC_000015.8 | Chr15 | 22,019,822 | 22,083,695 |