nsv4944
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:94,881
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 940 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 940 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 85 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4944 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 105,083,761 | 105,178,641 |
| nsv4944 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 104,419,462 | 104,514,342 |
| nsv4944 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000005.8 | Chr5 | 104,447,361 | 104,542,241 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3377 | Remapped | Perfect | NC_000005.10:g.(10 5083761_?)_(?_1051 78641)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 105,083,761 | 105,178,641 |
| nssv3377 | Remapped | Perfect | NC_000005.9:g.(104 419462_?)_(?_10451 4342)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 104,419,462 | 104,514,342 |
| nssv3377 | Submitted genomic | NC_000005.8:g.(104 447361_?)_(?_10454 2241)del71967 | NCBI35 (hg17) | NC_000005.8 | Chr5 | 104,447,361 | 104,542,241 |