nsv818547
- 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:163,250
- 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: 1771 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1771 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 42 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818547 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 111,438,856 | 111,602,105 |
| nsv818547 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 111,078,912 | 111,242,161 |
| nsv818547 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 110,672,863 | 110,836,112 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417387 | Remapped | Perfect | NC_000007.14:g.(?_ 111438856)_(111602 105_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 111,438,856 | 111,602,105 |
| nssv1417387 | Remapped | Perfect | NC_000007.13:g.(?_ 111078912)_(111242 161_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 111,078,912 | 111,242,161 |
| nssv1417387 | Submitted genomic | NC_000007.11:g.(?_ 110672863)_(110836 112_?)del | NCBI35 (hg17) | NC_000007.11 | Chr7 | 110,672,863 | 110,836,112 |