nsv1076328
- 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:93,302
- 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: 209 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 392 SVs from 51 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1076328 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NT_187513.1 | Unplaced|N T_187513.1 | 93,377 | 186,678 |
| nsv1076328 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 142,874,399 | 142,967,700 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3769735 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3769735 | Remapped | Perfect | NT_187513.1:g.9337 7_186678dup | GRCh38.p12 | First Pass | NT_187513.1 | Unplaced|N T_187513.1 | 93,377 | 186,678 |
| nssv3769735 | Submitted genomic | NC_000001.10:g.142 874399_142967700du p | GRCh37 (hg19) | NC_000001.10 | Chr1 | 142,874,399 | 142,967,700 |