nsv438237
- Organism: Homo sapiens
- Study:nstd20 (McCarroll et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:14,816
- Publication(s):McCarroll et al. 2006
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: 201 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 201 SVs from 37 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv438237 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 29,189,257 | 29,204,072 |
| nsv438237 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 29,412,123 | 29,426,938 |
| nsv438237 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | GPC_000000200.1 | Chr2 | 29,386,658 | 29,401,473 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv470308 | Remapped | Perfect | NC_000002.12:g.(?_ 29189257)_(2920407 2_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 29,189,257 | 29,204,072 |
| nssv470308 | Remapped | Perfect | NC_000002.11:g.(?_ 29412123)_(2942693 8_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 29,412,123 | 29,426,938 |
| nssv470308 | Submitted genomic | GPC_000000200.1:g. (?_29386658)_(2940 1473_?)del | NCBI34 (hg16) | GPC_000000200.1 | Chr2 | 29,386,658 | 29,401,473 |