nsv1154901
- Organism: Homo sapiens
- Study:nstd97 (Lou et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:116,291
- Publication(s):Lou et al. 2014
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: 532 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 532 SVs from 46 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv1154901 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 56,475,381 | 56,479,678 | 56,588,432 | 56,591,671 |
nsv1154901 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 57,049,515 | 57,053,812 | 57,162,566 | 57,165,805 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
nssv4008108 | deletion | SNP array | SNP genotyping analysis | 1 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv4008108 | Remapped | Perfect | NC_000013.11:g.(56 475381_56479678)_( 56588432_56591671) del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 56,475,381 | 56,479,678 | 56,588,432 | 56,591,671 |
nssv4008108 | Submitted genomic | NC_000013.10:g.(57 049515_57053812)_( 57162566_57165805) del | GRCh37 (hg19) | NC_000013.10 | Chr13 | 57,049,515 | 57,053,812 | 57,162,566 | 57,165,805 |