nsv818048
- 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:87,647
- 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: 311 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 311 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 7 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818048 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 73,998,307 | 74,085,953 |
| nsv818048 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 74,225,434 | 74,313,080 |
| nsv818048 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000002.9 | Chr2 | 74,137,089 | 74,224,735 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416317 | Remapped | Perfect | NC_000002.12:g.(?_ 73998307)_(7408595 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 73,998,307 | 74,085,953 |
| nssv1416317 | Remapped | Perfect | NC_000002.11:g.(?_ 74225434)_(7431308 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 74,225,434 | 74,313,080 |
| nssv1416317 | Submitted genomic | NC_000002.9:g.(?_7 4137089)_(74224735 _?)dup | NCBI35 (hg17) | NC_000002.9 | Chr2 | 74,137,089 | 74,224,735 |