nsv4386593
- 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:77,093
- 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: 407 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 412 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4386593 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 17,997,915 | 18,075,007 |
| nsv4386593 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 20,109,795 | 20,236,893 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15629768 | Remapped | Pass | NC_000024.10:g.(?_ 17997915)_(1807500 7_?)dup | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 17,997,915 | 18,075,007 |
| nssv15630541 | Remapped | Pass | NC_000024.10:g.(?_ 17997915)_(1807500 7_?)dup | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 17,997,915 | 18,075,007 |
| nssv15629768 | Submitted genomic | NC_000024.9:g.(?_2 0109795)_(20236893 _?)dup | GRCh37 (hg19) | NC_000024.9 | ChrY | 20,109,795 | 20,236,893 | ||
| nssv15630541 | Submitted genomic | NC_000024.9:g.(?_2 0109795)_(20236893 _?)dup | GRCh37 (hg19) | NC_000024.9 | ChrY | 20,109,795 | 20,236,893 |