nsv471376
- Organism: Homo sapiens
- Study:nstd31 (Alkan et al. 2009)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:47,848
- Description:CYFIP1
- Publication(s):Alkan et al. 2009
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: 1130 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 1431 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 59 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 |
---|---|---|---|---|---|---|---|---|---|
nsv471376 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 22,869,466 | 22,917,313 |
nsv471376 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 22,955,755 | 23,003,602 |
nsv471376 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 20,507,196 | 20,555,043 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv548106 | Remapped | Perfect | NC_000015.10:g.(22 869466_?)_(?_22917 313)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 22,869,466 | 22,917,313 |
nssv548106 | Remapped | Perfect | NC_000015.9:g.(229 55755_?)_(?_230036 02)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 22,955,755 | 23,003,602 |
nssv548106 | Submitted genomic | NC_000015.8:g.(205 07196_?)_(?_205550 43)del | NCBI35 (hg17) | NC_000015.8 | Chr15 | 20,507,196 | 20,555,043 |
Validation Information
Variant Call ID | Experiment ID | Sample ID | Method | Analysis | Result |
---|---|---|---|---|---|
nssv548106 | 4 | NA18507 | Oligo aCGH | Probe signal intensity | Pass |