nsv951195
- Organism: Homo sapiens
- Study:nstd73 (Dogan et al. 2014)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:99,600
- Publication(s):Dogan 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: 470 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 358 SVs from 48 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv951195 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 63,153,829 | 63,253,428 |
nsv951195 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 67,058,801 | 67,208,400 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv2996847 | deletion | SAMN01096093 | Sequencing | Read depth | 9,109 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv2996847 | Remapped | Pass | NC_000009.12:g.(63 153829_?)_(?_63253 428)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 63,153,829 | 63,253,428 |
nssv2996847 | Submitted genomic | NC_000009.11:g.(67 058801_?)_(?_67208 400)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 67,058,801 | 67,208,400 |