nsv1155647
- Organism: Homo sapiens
- Study:nstd97 (Lou et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:154,455
- Publication(s):Lou et al. 2014
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: 1331 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 1331 SVs from 78 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv1155647 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 15,028,408 | 15,033,451 | 15,181,285 | 15,182,862 |
nsv1155647 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 15,009,054 | 15,014,097 | 15,161,931 | 15,163,508 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
nssv4013878 | deletion | SNP array | SNP genotyping analysis | 1 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv4013878 | Remapped | Perfect | NC_000020.11:g.(15 028408_15033451)_( 15181285_15182862) del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 15,028,408 | 15,033,451 | 15,181,285 | 15,182,862 |
nssv4013878 | Submitted genomic | NC_000020.10:g.(15 009054_15014097)_( 15161931_15163508) del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 15,009,054 | 15,014,097 | 15,161,931 | 15,163,508 |