nsv8926
- Organism: Homo sapiens
- Study:nstd4 (Perry et al. 2008)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,850
- Publication(s):Perry et al. 2008
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: 103 SVs from 14 studies. See in: genome view
Overlapping variant regions from other studies: 104 SVs from 14 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv8926 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 18,391,169 | 18,411,018 |
nsv8926 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 18,544,103 | 18,563,952 |
nsv8926 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000012.9 | Chr12 | 18,435,370 | 18,455,219 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv19072 | Remapped | Perfect | NC_000012.12:g.(18 391169_18406824)_( 18407388_18411018) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 18,391,169 | 18,406,824 | 18,407,388 | 18,411,018 |
nssv19072 | Remapped | Perfect | NC_000012.11:g.(18 544103_18559758)_( 18560322_18563952) del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 18,544,103 | 18,559,758 | 18,560,322 | 18,563,952 |
nssv19072 | Submitted genomic | NC_000012.9:g.(184 35370_18451025)_(1 8451589_18455219)d el | NCBI35 (hg17) | NC_000012.9 | Chr12 | 18,435,370 | 18,451,025 | 18,451,589 | 18,455,219 |