nsv958982
- 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:42,492
- 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: 199 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv958982 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 31,064,469 | 31,106,960 |
| nsv958982 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 31,086,016 | 31,128,507 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020963 | deletion | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020963 | Remapped | Perfect | NC_000011.10:g.(30 952568_31064469)_( 31106960_31110260) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 30,952,568 | 31,064,469 | 31,106,960 | 31,110,260 |
| nssv3020963 | Submitted genomic | NC_000011.9:g.(309 74115_31086016)_(3 1128507_31131807)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 30,974,115 | 31,086,016 | 31,128,507 | 31,131,807 |