nsv2768221
- Organism: Homo sapiens
- Study:nstd125 (Wills et al. 2016)
- Variant Type:copy-neutral loss of heterozygosity
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,584,533
- Publication(s):Wills et al. 2016
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: 8060 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 8060 SVs from 106 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2768221 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 126,872,867 | 130,457,399 |
| nsv2768221 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 126,208,559 | 129,793,092 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv13638275 | copy-neutral loss of heterozygosity | 2 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv13638275 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 126,872,867 | 130,457,399 |
| nssv13638275 | Submitted genomic | GRCh37 (hg19) | NC_000005.9 | Chr5 | 126,208,559 | 129,793,092 |