nsv4385437
- 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:31,222
- 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: 220 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 221 SVs from 48 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4385437 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 77,647,457 | 77,678,678 |
| nsv4385437 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 77,276,774 | 77,307,995 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15657812 | Remapped | Perfect | NC_000007.14:g.(?_ 77647457)_(7767867 8_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 77,647,457 | 77,678,678 |
| nssv15663067 | Remapped | Perfect | NC_000007.14:g.(?_ 77647457)_(7767867 8_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 77,647,457 | 77,678,678 |
| nssv15657812 | Submitted genomic | NC_000007.13:g.(?_ 77276774)_(7730799 5_?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 77,276,774 | 77,307,995 | ||
| nssv15663067 | Submitted genomic | NC_000007.13:g.(?_ 77276774)_(7730799 5_?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 77,276,774 | 77,307,995 |