nsv949151
- 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:69,097
- 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: 256 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 256 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 14 SVs from 4 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 |
---|---|---|---|---|---|---|---|---|---|
nsv949151 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 28,097,196 | 28,166,292 |
nsv949151 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 28,386,125 | 28,455,221 |
nsv949151 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 28,426,131 | 28,495,227 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
nssv2767787 | copy number gain | SNP array | SNP genotyping analysis | 4 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv2767787 | Remapped | Perfect | NC_000010.11:g.(?_ 28097196)_(2816629 2_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 28,097,196 | 28,166,292 |
nssv2767787 | Remapped | Perfect | NC_000010.10:g.(?_ 28386125)_(2845522 1_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 28,386,125 | 28,455,221 |
nssv2767787 | Submitted genomic | NC_000010.8:g.(?_2 8426131)_(28495227 _?)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 28,426,131 | 28,495,227 |