nsv6636936
- 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:1,423,638
- Description:GRCh37/hg19 7q11.23(chr7:72718278-74142256)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: 4656 SVs from 103 studies. See in: genome view
Overlapping variant regions from other studies: 4647 SVs from 101 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6636936 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 73,304,281 | 74,727,918 |
| nsv6636936 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 72,718,278 | 74,142,256 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18329614 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV002472548.1, VCV001807742.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18329614 | Remapped | Good | NC_000007.14:g.(?_ 73304281)_(7472791 8_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 73,304,281 | 74,727,918 |
| nssv18329614 | Submitted genomic | NC_000007.13:g.(?_ 72718278)_(7414225 6_?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 72,718,278 | 74,142,256 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18329614 | GRCh37: NC_000007.13:g.(?_72718278)_(74142256_?)del | copy number loss | unknown | not provided | Pathogenic | ClinVar | RCV002472548.1, VCV001807742.1 | 1 |