nsv4457803
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:3,193,295
- Description:GRCh37/hg19 21q22.3(chr21:44310057-47503155)x1 AND not provided
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 15242 SVs from 119 studies. See in: genome view
Overlapping variant regions from other studies: 15319 SVs from 119 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4457803 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 42,889,947 | 46,083,241 |
| nsv4457803 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000021.8 | Chr21 | 44,310,057 | 47,503,155 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15777255 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV000847671.2, VCV000686963.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15777255 | Remapped | Good | NC_000021.9:g.(?_4 2889947)_(46083241 _?)del | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 42,889,947 | 46,083,241 |
| nssv15777255 | Submitted genomic | NC_000021.8:g.(?_4 4310057)_(47503155 _?)del | GRCh37 (hg19) | NC_000021.8 | Chr21 | 44,310,057 | 47,503,155 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15777255 | GRCh37: NC_000021.8:g.(?_44310057)_(47503155_?)del | copy number loss | unknown | not provided | Pathogenic | ClinVar | RCV000847671.2, VCV000686963.2 | 1 |