nsv4377776
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,519,158
- Publication(s):Zarrei et al. 2019
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: 17023 SVs from 123 studies. See in: genome view
Overlapping variant regions from other studies: 17024 SVs from 123 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4377776 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 86,436,852 | 92,956,009 |
| nsv4377776 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 86,980,083 | 93,499,239 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15655860 | copy number gain | 2-1743-004 | SNP array | Genotyping | 23 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15655860 | Remapped | Perfect | NC_000015.10:g.(?_ 86436852)_(9295600 9_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 86,436,852 | 92,956,009 |
| nssv15655860 | Submitted genomic | NC_000015.9:g.(?_8 6980083)_(93499239 _?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 86,980,083 | 93,499,239 |