nsv4369407
- 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:59,602
- 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: 685 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 685 SVs from 91 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4369407 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 38,283,338 | 38,342,939 |
| nsv4369407 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 38,322,939 | 38,382,540 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15612664 | Remapped | Perfect | NC_000007.14:g.(?_ 38283338)_(3834293 9_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 38,283,338 | 38,342,939 |
| nssv15702679 | Remapped | Perfect | NC_000007.14:g.(?_ 38283338)_(3834293 9_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 38,283,338 | 38,342,939 |
| nssv15612664 | Submitted genomic | NC_000007.13:g.(?_ 38322939)_(3838254 0_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 38,322,939 | 38,382,540 | ||
| nssv15702679 | Submitted genomic | NC_000007.13:g.(?_ 38322939)_(3838254 0_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 38,322,939 | 38,382,540 |