nsv1155018
- Organism: Homo sapiens
- Study:nstd97 (Lou et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:26
- Validation:Not tested
- Clinical Assertions: No
- Region Size:61,745
- 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: 687 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 687 SVs from 76 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1155018 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nsv1155018 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv4009423 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009424 | deletion | SNP array | SNP genotyping analysis | 0 |
| nssv4009425 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009426 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009427 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009428 | deletion | SNP array | SNP genotyping analysis | 0 |
| nssv4009429 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009430 | duplication | SNP array | SNP genotyping analysis | 3 |
| nssv4009431 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009432 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009433 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009434 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009435 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009436 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009437 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009438 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009439 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009440 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009441 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009442 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009443 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009444 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009445 | deletion | SNP array | SNP genotyping analysis | 0 |
| nssv4009446 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009447 | deletion | SNP array | SNP genotyping analysis | 1 |
| nssv4009448 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv4009423 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009424 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009425 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009426 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009427 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009428 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009429 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009430 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d up | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009431 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009432 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009433 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009434 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009435 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009436 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009437 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009438 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009439 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009440 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009441 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009442 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009443 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009444 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009445 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009446 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009447 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009448 | Remapped | Perfect | NC_000014.9:g.(411 39155_41141293)_(4 1188146_41200899)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,155 | 41,141,293 | 41,188,146 | 41,200,899 |
| nssv4009423 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009424 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009425 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009426 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009427 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009428 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009429 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009430 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d up | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009431 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009432 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009433 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009434 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009435 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009436 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009437 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009438 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009439 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009440 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009441 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009442 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009443 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009444 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009445 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009446 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009447 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 | ||
| nssv4009448 | Submitted genomic | NC_000014.8:g.(416 08358_41610496)_(4 1657349_41670102)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 41,608,358 | 41,610,496 | 41,657,349 | 41,670,102 |