nsv4383493
- 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:16,865
- 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: 224 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 263 SVs from 48 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4383493 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 145,198,832 | 145,215,696 |
| nsv4383493 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 144,323,717 | 144,352,893 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15622135 | Remapped | Pass | NC_000001.11:g.(?_ 145198832)_(145215 696_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 145,198,832 | 145,215,696 |
| nssv15696899 | Remapped | Pass | NC_000001.11:g.(?_ 145198832)_(145215 696_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 145,198,832 | 145,215,696 |
| nssv15622135 | Submitted genomic | NC_000001.10:g.(?_ 144323717)_(144352 893_?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 144,323,717 | 144,352,893 | ||
| nssv15696899 | Submitted genomic | NC_000001.10:g.(?_ 144323717)_(144352 893_?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 144,323,717 | 144,352,893 |