nsv4381987
- 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:307,590
- 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: 1643 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1512 SVs from 92 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4381987 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 35,232,320 | 35,539,909 |
| nsv4381987 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 34,466,691 | 34,774,280 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15684093 | Remapped | Perfect | NC_000016.10:g.(?_ 35232320)_(3553990 9_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,232,320 | 35,539,909 |
| nssv15699628 | Remapped | Perfect | NC_000016.10:g.(?_ 35232320)_(3553990 9_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,232,320 | 35,539,909 |
| nssv15684093 | Submitted genomic | NC_000016.9:g.(?_3 4466691)_(34774280 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,466,691 | 34,774,280 | ||
| nssv15699628 | Submitted genomic | NC_000016.9:g.(?_3 4466691)_(34774280 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,466,691 | 34,774,280 |