nsv2768211
- 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:3,171,849
- 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: 9229 SVs from 123 studies. See in: genome view
Overlapping variant regions from other studies: 9229 SVs from 123 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 |
---|---|---|---|---|---|---|---|---|---|
nsv2768211 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 38,154,063 | 41,325,911 |
nsv2768211 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 38,381,205 | 41,553,051 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv13638298 | copy-neutral loss of heterozygosity | 16 | SNP array | SNP genotyping analysis | nssv13638297 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|
nssv13638298 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 38,154,063 | 41,325,911 |
nssv13638298 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 38,381,205 | 41,553,051 |