nsv958969
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:167,495
- Publication(s):Poultney et al. 2013
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: 401 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 401 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv958969 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 77,477,412 | 77,644,906 |
| nsv958969 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 77,526,563 | 77,694,057 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021927 | duplication | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021927 | Remapped | Perfect | NC_000003.12:g.(77 098342_77098342)_( 78598913_78598913) dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 77,098,342 | 77,098,342 | 78,598,913 | 78,598,913 |
| nssv3021927 | Submitted genomic | NC_000003.11:g.(77 147493_77526563)_( 77694057_78648063) dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 77,147,493 | 77,526,563 | 77,694,057 | 78,648,063 |