nsv3967798
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:copy number variation
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,910
- Publication(s):Levy-Sakin et al. 2019
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: 114 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 114 SVs from 30 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3967798 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 59,505,129 | 59,527,038 | ||
nsv3967798 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 59,272,602 | 59,294,511 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15211261 | deletion | Optical mapping | Optical mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15211261 | Submitted genomic | NC_000011.10:g.(59 505129_?)_(?_59527 038)del | GRCh38 (hg38) | NC_000011.10 | Chr11 | 59,505,129 | 59,527,038 | ||
nssv15211261 | Remapped | Perfect | NC_000011.9:g.(592 72602_?)_(?_592945 11)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 59,272,602 | 59,294,511 |