nsv959800
- 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:55,821
- 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: 341 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 341 SVs from 46 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959800 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 33,293,157 | 33,348,977 |
| nsv959800 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 30,873,121 | 30,928,941 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021580 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021580 | Remapped | Perfect | NC_000018.10:g.(33 267299_33293157)_( 33348977_33370048) del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 33,267,299 | 33,293,157 | 33,348,977 | 33,370,048 |
| nssv3021580 | Submitted genomic | NC_000018.9:g.(308 47263_30873121)_(3 0928941_30950012)d el | GRCh37 (hg19) | NC_000018.9 | Chr18 | 30,847,263 | 30,873,121 | 30,928,941 | 30,950,012 |