nsv4452263
- 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:345,759
- Description:GRCh37/hg19 2q24.1(chr2:157124370-157470128)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: 857 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 857 SVs from 61 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4452263 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 156,267,858 | 156,613,616 |
| nsv4452263 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 157,124,370 | 157,470,128 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15772330 | copy number loss | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000847405.2, VCV000686697.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15772330 | Remapped | Perfect | NC_000002.12:g.(?_ 156267858)_(156613 616_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 156,267,858 | 156,613,616 |
| nssv15772330 | Submitted genomic | NC_000002.11:g.(?_ 157124370)_(157470 128_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 157,124,370 | 157,470,128 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15772330 | GRCh37: NC_000002.11:g.(?_157124370)_(157470128_?)del | copy number loss | unknown | not provided | Uncertain significance | ClinVar | RCV000847405.2, VCV000686697.2 | 1 |