nsv833676
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:223,533
- Publication(s):Wong 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: 1452 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1452 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 120 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv833676 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 65,836,022 | 66,059,554 |
| nsv833676 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 63,503,258 | 63,726,790 |
| nsv833676 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000018.8 | Chr18 | 61,654,238 | 61,877,770 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1454061 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1454062 | copy number gain | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1454061 | Remapped | Perfect | NC_000018.10:g.(65 836022_?)_(?_66059 554)dup | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 65,836,022 | 66,059,554 |
| nssv1454062 | Remapped | Perfect | NC_000018.10:g.(65 836022_?)_(?_66059 554)dup | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 65,836,022 | 66,059,554 |
| nssv1454061 | Remapped | Perfect | NC_000018.9:g.(635 03258_?)_(?_637267 90)dup | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 63,503,258 | 63,726,790 |
| nssv1454062 | Remapped | Perfect | NC_000018.9:g.(635 03258_?)_(?_637267 90)dup | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 63,503,258 | 63,726,790 |
| nssv1454061 | Submitted genomic | NC_000018.8:g.(616 54238_?)_(?_618777 70)dup | NCBI35 (hg17) | NC_000018.8 | Chr18 | 61,654,238 | 61,877,770 | ||
| nssv1454062 | Submitted genomic | NC_000018.8:g.(616 54238_?)_(?_618777 70)dup | NCBI35 (hg17) | NC_000018.8 | Chr18 | 61,654,238 | 61,877,770 |