nsv482903
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:150,441
- Publication(s):Sharp 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: 636 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 636 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482903 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 10,771,224 | 10,921,664 |
| nsv482903 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 10,771,336 | 10,921,776 |
| nsv482903 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000005.7 | Chr5 | 10,824,074 | 10,974,514 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3008430 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv3010723 | copy number gain | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3008430 | Remapped | Perfect | NC_000005.10:g.(?_ 10771224)_(1092166 4_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 10,771,224 | 10,921,664 |
| nssv3010723 | Remapped | Perfect | NC_000005.10:g.(?_ 10771224)_(1092166 4_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 10,771,224 | 10,921,664 |
| nssv3008430 | Remapped | Perfect | NC_000005.9:g.(?_1 0771336)_(10921776 _?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 10,771,336 | 10,921,776 |
| nssv3010723 | Remapped | Perfect | NC_000005.9:g.(?_1 0771336)_(10921776 _?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 10,771,336 | 10,921,776 |
| nssv3008430 | Submitted genomic | NC_000005.7:g.(?_1 0824074)_(10974514 _?)dup | NCBI34 (hg16) | NC_000005.7 | Chr5 | 10,824,074 | 10,974,514 | ||
| nssv3010723 | Submitted genomic | NC_000005.7:g.(?_1 0824074)_(10974514 _?)dup | NCBI34 (hg16) | NC_000005.7 | Chr5 | 10,824,074 | 10,974,514 |