nsv3924892
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38, NCBI36
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:581,062
- Description:GRCh38/hg38 14q12(chr14:26741728-27322789)x1 AND See cases
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1879 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1879 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 464 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3924892 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000014.9 | Chr14 | 26,741,728 | 27,322,789 |
| nsv3924892 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 27,210,934 | 27,791,995 |
| nsv3924892 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 26,280,774 | 26,861,835 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15137434 | copy number loss | Multiple | Multiple | See cases | Likely benign | ClinVar | RCV000140910.5, VCV000152352.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15137434 | Submitted genomic | NC_000014.9:g.(?_2 6741728)_(27322789 _?)del | GRCh38 (hg38) | NC_000014.9 | Chr14 | 26,741,728 | 27,322,789 |
| nssv15137434 | Submitted genomic | NC_000014.8:g.(?_2 7210934)_(27791995 _?)del | GRCh37 (hg19) | NC_000014.8 | Chr14 | 27,210,934 | 27,791,995 |
| nssv15137434 | Submitted genomic | NC_000014.7:g.(?_2 6280774)_(26861835 _?)del | NCBI36 (hg18) | NC_000014.7 | Chr14 | 26,280,774 | 26,861,835 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15137434 | GRCh37: NC_000014.8:g.(?_27210934)_(27791995_?)del, GRCh38: NC_000014.9:g.(?_26741728)_(27322789_?)del, NCBI36: NC_000014.7:g.(?_26280774)_(26861835_?)del | copy number loss | maternal | See cases | Likely benign | ClinVar | RCV000140910.5, VCV000152352.2 | 1 |