nsv949582
- Organism: Homo sapiens
- Study:nstd85 (vanSilfhout et al. 2013)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:239,531
- Publication(s):Vulto-van Silfhout et al. 2013
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: 930 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 930 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 42 SVs from 2 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv949582 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 91,410,077 | 91,649,607 |
| nsv949582 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 92,062,331 | 92,301,861 |
| nsv949582 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000013.9 | Chr13 | 90,860,332 | 91,099,862 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv2768311 | copy number loss | SNP array | SNP genotyping analysis | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2768311 | Remapped | Perfect | NC_000013.11:g.(?_ 91410077)_(9164960 7_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 91,410,077 | 91,649,607 |
| nssv2768311 | Remapped | Perfect | NC_000013.10:g.(?_ 92062331)_(9230186 1_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 92,062,331 | 92,301,861 |
| nssv2768311 | Submitted genomic | NC_000013.9:g.(?_9 0860332)_(91099862 _?)del | NCBI35 (hg17) | NC_000013.9 | Chr13 | 90,860,332 | 91,099,862 |