nsv4372435
- 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:24,604
- 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: 180 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 376 SVs from 60 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4372435 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | First Pass | NT_187614.1 | Chr17|NT_1 87614.1 | 2,229,663 | 2,254,266 |
| nsv4372435 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 36,350,598 | 36,375,201 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15651258 | Remapped | Perfect | NT_187614.1:g.(?_2 229663)_(2254266_? )dup | GRCh38.p12 | First Pass | NT_187614.1 | Chr17|NT_1 87614.1 | 2,229,663 | 2,254,266 |
| nssv15682213 | Remapped | Perfect | NT_187614.1:g.(?_2 229663)_(2254266_? )dup | GRCh38.p12 | First Pass | NT_187614.1 | Chr17|NT_1 87614.1 | 2,229,663 | 2,254,266 |
| nssv15651258 | Submitted genomic | NC_000017.10:g.(?_ 36350598)_(3637520 1_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 36,350,598 | 36,375,201 | ||
| nssv15682213 | Submitted genomic | NC_000017.10:g.(?_ 36350598)_(3637520 1_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 36,350,598 | 36,375,201 |