nsv818029
- 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:150,854
- 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: 595 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 595 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 67 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818029 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 64,416,679 | 64,567,532 |
| nsv818029 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 63,636,559 | 63,787,412 |
| nsv818029 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 63,419,580 | 63,570,433 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416997 | Remapped | Perfect | NC_000023.11:g.(?_ 64416679)_(6456753 2_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 64,416,679 | 64,567,532 |
| nssv1416997 | Remapped | Perfect | NC_000023.10:g.(?_ 63636559)_(6378741 2_?)dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 63,636,559 | 63,787,412 |
| nssv1416997 | Submitted genomic | NC_000023.8:g.(?_6 3419580)_(63570433 _?)dup | NCBI35 (hg17) | NC_000023.8 | ChrX | 63,419,580 | 63,570,433 |