nsv482877
- 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:178,384
- 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: 434 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 434 SVs from 60 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 |
---|---|---|---|---|---|---|---|---|---|
nsv482877 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 91,217,069 | 91,395,452 |
nsv482877 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 93,979,351 | 94,157,734 |
nsv482877 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | GPC_000000201.1 | Chr9 | 89,320,760 | 89,499,143 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3010261 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv3010261 | Remapped | Perfect | NC_000009.12:g.(?_ 91217069)_(9139545 2_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 91,217,069 | 91,395,452 |
nssv3010261 | Remapped | Perfect | NC_000009.11:g.(?_ 93979351)_(9415773 4_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 93,979,351 | 94,157,734 |
nssv3010261 | Submitted genomic | GPC_000000201.1:g. (?_89320760)_(8949 9143_?)dup | NCBI34 (hg16) | GPC_000000201.1 | Chr9 | 89,320,760 | 89,499,143 |