nsv9492
- Organism: Homo sapiens
- Study:nstd4 (Perry et al. 2008)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:59,850
- Publication(s):Perry et al. 2008
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: 66 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 66 SVs from 18 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 |
---|---|---|---|---|---|---|---|---|---|
nsv9492 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 11,134,540 | 11,194,389 |
nsv9492 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 11,037,857 | 11,097,706 |
nsv9492 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000017.9 | Chr17 | 10,978,582 | 11,038,431 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv28167 | Remapped | Perfect | NC_000017.11:g.(11 134540_11135515)_( 11137783_11194389) del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 11,134,540 | 11,135,515 | 11,137,783 | 11,194,389 |
nssv28167 | Remapped | Perfect | NC_000017.10:g.(11 037857_11038832)_( 11041100_11097706) del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 11,037,857 | 11,038,832 | 11,041,100 | 11,097,706 |
nssv28167 | Submitted genomic | NC_000017.9:g.(109 78582_10979557)_(1 0981825_11038431)d el | NCBI35 (hg17) | NC_000017.9 | Chr17 | 10,978,582 | 10,979,557 | 10,981,825 | 11,038,431 |