nsv482846
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:167,686
- 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: 535 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 533 SVs from 59 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 |
---|---|---|---|---|---|---|---|---|---|
nsv482846 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 101,896,701 | 102,064,386 |
nsv482846 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 101,539,981 | 101,707,666 |
nsv482846 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000007.10 | Chr7 | 101,100,162 | 101,267,847 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3007553 | copy number loss | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv3007553 | Remapped | Perfect | NC_000007.14:g.(?_ 101896701)_(102064 386_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 101,896,701 | 102,064,386 |
nssv3007553 | Remapped | Perfect | NC_000007.13:g.(?_ 101539981)_(101707 666_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 101,539,981 | 101,707,666 |
nssv3007553 | Submitted genomic | NC_000007.10:g.(?_ 101100162)_(101267 847_?)del | NCBI34 (hg16) | NC_000007.10 | Chr7 | 101,100,162 | 101,267,847 |