nsv4372114
- 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:86,606
- 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: 866 SVs from 100 studies. See in: genome view
Overlapping variant regions from other studies: 866 SVs from 100 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4372114 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 38,244,586 | 38,331,191 |
| nsv4372114 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 38,284,187 | 38,370,792 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15629667 | Remapped | Perfect | NC_000007.14:g.(?_ 38244586)_(3833119 1_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 38,244,586 | 38,331,191 |
| nssv15644057 | Remapped | Perfect | NC_000007.14:g.(?_ 38244586)_(3833119 1_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 38,244,586 | 38,331,191 |
| nssv15629667 | Submitted genomic | NC_000007.13:g.(?_ 38284187)_(3837079 2_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 38,284,187 | 38,370,792 | ||
| nssv15644057 | Submitted genomic | NC_000007.13:g.(?_ 38284187)_(3837079 2_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 38,284,187 | 38,370,792 |