nsv3915279
- 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:15,038,781
- Description:GRCh38/hg38 18p11.32-11.21(chr18:136226-15175006) 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: 46511 SVs from 130 studies. See in: genome view
Overlapping variant regions from other studies: 46517 SVs from 130 studies. See in: genome view
Overlapping variant regions from other studies: 12404 SVs from 39 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3915279 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000018.10 | Chr18 | 136,226 | 15,175,006 |
| nsv3915279 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 136,226 | 15,175,005 |
| nsv3915279 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 126,226 | 15,165,005 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv15148900 | copy number gain | Multiple | Multiple | See cases | Pathogenic | ClinVar | RCV000140442.5, VCV000151749.2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15148900 | Submitted genomic | NC_000018.10:g.(?_ 136226)_(15175006_ ?)dup | GRCh38 (hg38) | NC_000018.10 | Chr18 | 136,226 | 15,175,006 |
| nssv15148900 | Submitted genomic | NC_000018.9:g.(?_1 36226)_(15175005_? )dup | GRCh37 (hg19) | NC_000018.9 | Chr18 | 136,226 | 15,175,005 |
| nssv15148900 | Submitted genomic | NC_000018.8:g.(?_1 26226)_(15165005_? )dup | NCBI36 (hg18) | NC_000018.8 | Chr18 | 126,226 | 15,165,005 |
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 |
|---|---|---|---|---|---|---|---|
| nssv15148900 | GRCh37: NC_000018.9:g.(?_136226)_(15175005_?)dup, GRCh38: NC_000018.10:g.(?_136226)_(15175006_?)dup, NCBI36: NC_000018.8:g.(?_126226)_(15165005_?)dup | copy number gain | not provided | See cases | Pathogenic | ClinVar | RCV000140442.5, VCV000151749.2 |