nsv3922745
- 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:51,452,664
- Description:GRCh38/hg38 4q31.1-35.2(chr4:138510532-189963195)x3 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: 157441 SVs from 148 studies. See in: genome view
Overlapping variant regions from other studies: 157207 SVs from 148 studies. See in: genome view
Overlapping variant regions from other studies: 41027 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3922745 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000004.12 | Chr4 | 138,510,532 | 189,963,195 |
| nsv3922745 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 139,431,686 | 190,828,225 |
| nsv3922745 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 139,651,136 | 191,121,344 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15136235 | copy number gain | Multiple | Multiple | See cases | Pathogenic | ClinVar | RCV000136810.4, VCV000147647.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15136235 | Submitted genomic | NC_000004.12:g.(?_ 138510532)_(189963 195_?)dup | GRCh38 (hg38) | NC_000004.12 | Chr4 | 138,510,532 | 189,963,195 |
| nssv15136235 | Submitted genomic | NC_000004.11:g.(?_ 139431686)_(190828 225_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 139,431,686 | 190,828,225 |
| nssv15136235 | Submitted genomic | NC_000004.10:g.(?_ 139651136)_(191121 344_?)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 139,651,136 | 191,121,344 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15136235 | GRCh37: NC_000004.11:g.(?_139431686)_(190828225_?)dup, GRCh38: NC_000004.12:g.(?_138510532)_(189963195_?)dup, NCBI36: NC_000004.10:g.(?_139651136)_(191121344_?)dup | copy number gain | not provided | See cases | Pathogenic | ClinVar | RCV000136810.4, VCV000147647.2 | 3 |