nsv1076363
- Organism: Homo sapiens
- Study:nstd99 (Thareja et al. 2015)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:79,644
- Publication(s):Thareja et al. 2015
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: 801 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 443 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 849 SVs from 68 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1076363 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 42,113,251 | 42,191,852 |
| nsv1076363 | Remapped | Good | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187579.1 | Chr10|NT_1 87579.1 | 10,012 | 89,655 |
| nsv1076363 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 42,608,699 | 42,687,300 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3766710 | duplication | KWP1 | Sequencing | Read depth and paired-end mapping | 11,116 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3766710 | Remapped | Good | NT_187579.1:g.1001 2_89655dup | GRCh38.p12 | Second Pass | NT_187579.1 | Chr10|NT_1 87579.1 | 10,012 | 89,655 |
| nssv3766710 | Remapped | Perfect | NC_000010.11:g.421 13251_42191852dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 42,113,251 | 42,191,852 |
| nssv3766710 | Submitted genomic | NC_000010.10:g.426 08699_42687300dup | GRCh37 (hg19) | NC_000010.10 | Chr10 | 42,608,699 | 42,687,300 |