nsv4374567
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,962,561
- 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: 8839 SVs from 117 studies. See in: genome view
Overlapping variant regions from other studies: 8971 SVs from 117 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4374567 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 32,016,644 | 33,979,204 |
| nsv4374567 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 32,027,965 | 33,781,671 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15621726 | Remapped | Pass | NC_000016.10:g.(?_ 32016644)_(3397920 4_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,016,644 | 33,979,204 |
| nssv15641196 | Remapped | Pass | NC_000016.10:g.(?_ 32016644)_(3397920 4_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,016,644 | 33,979,204 |
| nssv15621726 | Submitted genomic | NC_000016.9:g.(?_3 2027965)_(33781671 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 32,027,965 | 33,781,671 | ||
| nssv15641196 | Submitted genomic | NC_000016.9:g.(?_3 2027965)_(33781671 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 32,027,965 | 33,781,671 |