nsv958905
- 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:64,886
- 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: 285 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 287 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv958905 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 174,637,373 | 174,702,258 |
| nsv958905 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 174,606,511 | 174,671,396 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021082 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021082 | Remapped | Perfect | NC_000001.11:g.(17 4449199_174637373) _(174702258_174752 311)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 174,449,199 | 174,637,373 | 174,702,258 | 174,752,311 |
| nssv3021082 | Submitted genomic | NC_000001.10:g.(17 4418337_174606511) _(174671396_174721 449)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 174,418,337 | 174,606,511 | 174,671,396 | 174,721,449 |