nsv818507
- 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:96,854
- 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: 547 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 545 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 15 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818507 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 57,729,825 | 57,826,678 |
| nsv818507 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 57,789,531 | 57,886,384 |
| nsv818507 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 57,600,188 | 57,697,041 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418160 | Remapped | Perfect | NC_000007.14:g.(?_ 57729825)_(5782667 8_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 57,729,825 | 57,826,678 |
| nssv1418160 | Remapped | Perfect | NC_000007.13:g.(?_ 57789531)_(5788638 4_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 57,789,531 | 57,886,384 |
| nssv1418160 | Submitted genomic | NC_000007.11:g.(?_ 57600188)_(5769704 1_?)dup | NCBI35 (hg17) | NC_000007.11 | Chr7 | 57,600,188 | 57,697,041 |