nsv433226
- 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:73,645
- 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: 459 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 459 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 30 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433226 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 13,097,593 | 13,171,237 |
| nsv433226 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 13,097,705 | 13,171,349 |
| nsv433226 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000005.8 | Chr5 | 13,150,705 | 13,224,349 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463107 | Remapped | Perfect | NC_000005.10:g.(?_ 13097593)_(1317123 7_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 13,097,593 | 13,171,237 |
| nssv463107 | Remapped | Perfect | NC_000005.9:g.(?_1 3097705)_(13171349 _?)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 13,097,705 | 13,171,349 |
| nssv463107 | Submitted genomic | NC_000005.8:g.(?_1 3150705)_(13224349 _?)del | NCBI35 (hg17) | NC_000005.8 | Chr5 | 13,150,705 | 13,224,349 |