nsv818359
- 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:90,243
- 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: 381 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 381 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818359 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 98,111,891 | 98,202,133 |
| nsv818359 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 97,447,595 | 97,537,837 |
| nsv818359 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000005.8 | Chr5 | 97,473,351 | 97,563,593 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416735 | Remapped | Perfect | NC_000005.10:g.(?_ 98111891)_(9820213 3_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 98,111,891 | 98,202,133 |
| nssv1416735 | Remapped | Perfect | NC_000005.9:g.(?_9 7447595)_(97537837 _?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 97,447,595 | 97,537,837 |
| nssv1416735 | Submitted genomic | NC_000005.8:g.(?_9 7473351)_(97563593 _?)dup | NCBI35 (hg17) | NC_000005.8 | Chr5 | 97,473,351 | 97,563,593 |