nsv3923911
- 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:30,099,563
- Description:GRCh38/hg38 13q13.3-21.32(chr13:37864226-67963788)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: 78654 SVs from 138 studies. See in: genome view
Overlapping variant regions from other studies: 78670 SVs from 138 studies. See in: genome view
Overlapping variant regions from other studies: 21234 SVs from 36 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3923911 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 37,864,226 | 67,963,788 |
| nsv3923911 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 38,438,363 | 68,537,920 |
| nsv3923911 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 37,336,363 | 67,435,921 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15147516 | copy number loss | Multiple | Multiple | See cases | Pathogenic | ClinVar | RCV000140744.5, VCV000152095.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15147516 | Submitted genomic | NC_000013.11:g.(?_ 37864226)_(6796378 8_?)del | GRCh38 (hg38) | NC_000013.11 | Chr13 | 37,864,226 | 67,963,788 |
| nssv15147516 | Submitted genomic | NC_000013.10:g.(?_ 38438363)_(6853792 0_?)del | GRCh37 (hg19) | NC_000013.10 | Chr13 | 38,438,363 | 68,537,920 |
| nssv15147516 | Submitted genomic | NC_000013.9:g.(?_3 7336363)_(67435921 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 37,336,363 | 67,435,921 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15147516 | GRCh37: NC_000013.10:g.(?_38438363)_(68537920_?)del, GRCh38: NC_000013.11:g.(?_37864226)_(67963788_?)del, NCBI36: NC_000013.9:g.(?_37336363)_(67435921_?)del | copy number loss | not provided | See cases | Pathogenic | ClinVar | RCV000140744.5, VCV000152095.2 | 1 |