nsv2768210
- 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:3,155,971
- 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: 6988 SVs from 110 studies. See in: genome view
Overlapping variant regions from other studies: 6988 SVs from 110 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2768210 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 134,160,982 | 137,316,952 |
| nsv2768210 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 134,918,553 | 138,074,522 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv13638297 | copy-neutral loss of heterozygosity | 16 | SNP array | SNP genotyping analysis | nssv13638298 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv13638297 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 134,160,982 | 137,316,952 |
| nssv13638297 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 134,918,553 | 138,074,522 |