nsv433374
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:58,239
- Publication(s):Cooper et al. 2008
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: 532 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 532 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 36 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433374 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 176,144,148 | 176,202,386 |
| nsv433374 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 175,571,151 | 175,629,389 |
| nsv433374 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000005.8 | Chr5 | 175,503,757 | 175,561,995 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463255 | Remapped | Perfect | NC_000005.10:g.(?_ 176144148)_(176202 386_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 176,144,148 | 176,202,386 |
| nssv463255 | Remapped | Perfect | NC_000005.9:g.(?_1 75571151)_(1756293 89_?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 175,571,151 | 175,629,389 |
| nssv463255 | Submitted genomic | NC_000005.8:g.(?_1 75503757)_(1755619 95_?)dup | NCBI35 (hg17) | NC_000005.8 | Chr5 | 175,503,757 | 175,561,995 |