nsv4708861
- Organism: Homo sapiens
- Study:nstd195 (Mwapagha et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:701
- Publication(s):Mwapagha et al. 2021
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: 25 SVs from 9 studies. See in: genome view
Overlapping variant regions from other studies: 446 SVs from 57 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4708861 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | First Pass | NT_187524.1 | Chr2|NT_18 7524.1 | 20,138 | 20,838 |
| nsv4708861 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 91,613,151 | 91,613,851 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| nssv16240631 | copy number variation | M478 | Sequencing | Paired-end mapping | 3 | 4,557 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv16240631 | Remapped | Perfect | GRCh38.p12 | First Pass | NT_187524.1 | Chr2|NT_18 7524.1 | 20,138 | 20,838 |
| nssv16240631 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 91,613,151 | 91,613,851 |