nsv6637155
- 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:302,232
- Description:GRCh37/hg19 6q21(chr6:109576603-109878834)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: 713 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 713 SVs from 62 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637155 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 109,255,400 | 109,557,631 |
| nsv6637155 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 109,576,603 | 109,878,834 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330742 | copy number loss | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002472603.1, VCV001807797.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330742 | Remapped | Perfect | NC_000006.12:g.(?_ 109255400)_(109557 631_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 109,255,400 | 109,557,631 |
| nssv18330742 | Submitted genomic | NC_000006.11:g.(?_ 109576603)_(109878 834_?)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 109,576,603 | 109,878,834 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330742 | GRCh37: NC_000006.11:g.(?_109576603)_(109878834_?)del | copy number loss | unknown | not provided | Uncertain significance | ClinVar | RCV002472603.1, VCV001807797.1 | 1 |