nsv1067823
- Organism: Homo sapiens
- Study:nstd98 (Campbell et al. 2014b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:876,783
- Publication(s):Campbell 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: 2183 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 2183 SVs from 98 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067823 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 77,091,143 | 77,091,192 | 77,967,876 | 77,967,925 |
| nsv1067823 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 77,318,269 | 77,318,318 | 78,195,002 | 78,195,051 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761533 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761533 | Remapped | Perfect | NC_000002.12:g.(77 091143_77091192)_( 77967876_77967925) dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 77,091,143 | 77,091,192 | 77,967,876 | 77,967,925 |
| nssv3761533 | Submitted genomic | NC_000002.11:g.(77 318269_77318318)_( 78195002_78195051) dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 77,318,269 | 77,318,318 | 78,195,002 | 78,195,051 |