nsv4679126
- Organism: Homo sapiens
- Study:nstd189 (Perez-Palma et al. 2020)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,531,064
- Publication(s):Pérez-Palma et al. 2020
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: 6806 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 6806 SVs from 95 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4679126 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 44,081,707 | 46,612,770 |
| nsv4679126 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000013.10 | Chr13 | 44,655,843 | 47,186,905 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16210870 | deletion | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16210870 | Remapped | Perfect | NC_000013.11:g.(?_ 44081707)_(4661277 0_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 44,081,707 | 46,612,770 |
| nssv16210870 | Submitted genomic | NC_000013.10:g.(?_ 44655843)_(4718690 5_?)del | GRCh37.p13 | NC_000013.10 | Chr13 | 44,655,843 | 47,186,905 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) |
|---|---|
| nssv16210870 | <0.001 |