nsv3117732
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,491
- Publication(s):Lu et al. 2017
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: 252 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 252 SVs from 66 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3117732 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 91,408,691 | 91,413,181 |
nsv3117732 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 91,038,006 | 91,042,496 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14084273 | Remapped | Perfect | NC_000007.14:g.(?_ 91408691)_(9141318 1_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 91,408,691 | 91,413,181 |
nssv14084798 | Remapped | Perfect | NC_000007.14:g.(?_ 91408691)_(9141318 1_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 91,408,691 | 91,413,181 |
nssv14084273 | Submitted genomic | NC_000007.13:g.(?_ 91038006)_(9104249 6_?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 91,038,006 | 91,042,496 | ||
nssv14084798 | Submitted genomic | NC_000007.13:g.(?_ 91038006)_(9104249 6_?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 91,038,006 | 91,042,496 |