nsv932797
- Organism: Homo sapiens
- Study:nstd79 (Dittwald et al. 2013)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,949,088
- Publication(s):Dittwald et al. 2013
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: 10858 SVs from 125 studies. See in: genome view
Overlapping variant regions from other studies: 10860 SVs from 125 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv932797 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 74,051,746 | 74,051,746 | 78,000,833 | 78,000,833 |
| nsv932797 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 74,344,087 | 74,412,642 | 78,151,253 | 78,293,175 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv1610951 | deletion | 60 | Oligo aCGH | Probe signal intensity |
| nssv1611391 | deletion | 1990 | Oligo aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1610951 | Remapped | Perfect | NC_000015.10:g.(74 172899_74172899)_( 77858407_77858407) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 74,172,899 | 74,172,899 | 77,858,407 | 77,858,407 |
| nssv1611391 | Remapped | Perfect | NC_000015.10:g.(74 203105_74203105)_( 78001369_78001369) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 74,203,105 | 74,203,105 | 78,001,369 | 78,001,369 |
| nssv1610951 | Remapped | Perfect | NC_000015.9:g.(744 65240_74465240)_(7 8150749_78150749)d el | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 74,465,240 | 74,465,240 | 78,150,749 | 78,150,749 |
| nssv1611391 | Submitted genomic | NC_000015.9:g.(744 95446_74495507)_(7 8150795_78293711)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 74,495,446 | 74,495,507 | 78,150,795 | 78,293,711 | ||
| nssv1610951 | Submitted genomic | NC_000015.8:g.(722 52293_72253337)_(7 5934113_75937804)d el | NCBI36 (hg18) | NC_000015.8 | Chr15 | 72,252,293 | 72,253,337 | 75,934,113 | 75,937,804 |