nsv429501
- Organism: Homo sapiens
- Study:nstd11 (Walter et al. 2009)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:35,143,784
- Publication(s):Walter et al. 2009
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 110321 SVs from 141 studies. See in: genome view
Overlapping variant regions from other studies: 110432 SVs from 141 studies. See in: genome view
Overlapping variant regions from other studies: 32354 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv429501 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 43,902 | 35,187,685 |
| nsv429501 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 10,239 | 35,227,297 |
| nsv429501 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 52,911 | 35,193,822 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|---|
| nssv459287 | copy number loss | SNP array | SNP genotyping analysis | Leukemia, Myeloid, Acute | not provided | Submitter |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv459287 | Remapped | Good | NC_000007.14:g.(?_ 43902)_(35187685_? )del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 43,902 | 35,187,685 |
| nssv459287 | Remapped | Good | NC_000007.13:g.(?_ 10239)_(35227297_? )del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 10,239 | 35,227,297 |
| nssv459287 | Submitted genomic | NC_000007.12:g.(?_ 52911)_(35193822_? )del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 52,911 | 35,193,822 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|---|
| nssv459287 | NCBI36: NC_000007.12:g.(?_52911)_(35193822_?)del | copy number loss | somatic | Leukemia, Myeloid, Acute | not provided | Submitter |