nsv818290
- 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:96,790
- 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: 1022 SVs from 100 studies. See in: genome view
Overlapping variant regions from other studies: 1022 SVs from 100 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 12 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818290 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 160,909,586 | 161,006,375 |
| nsv818290 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 161,830,738 | 161,927,527 |
| nsv818290 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000004.9 | Chr4 | 162,188,343 | 162,285,132 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417722 | Remapped | Perfect | NC_000004.12:g.(?_ 160909586)_(161006 375_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 160,909,586 | 161,006,375 |
| nssv1417722 | Remapped | Perfect | NC_000004.11:g.(?_ 161830738)_(161927 527_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 161,830,738 | 161,927,527 |
| nssv1417722 | Submitted genomic | NC_000004.9:g.(?_1 62188343)_(1622851 32_?)dup | NCBI35 (hg17) | NC_000004.9 | Chr4 | 162,188,343 | 162,285,132 |