nsv6290103
- Organism: Homo sapiens
- Study:nstd218 (Wijesiriwardhana et al. 2021)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:88,257
- Publication(s):Wijesiriwardhana et al. 2021
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: 453 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 453 SVs from 58 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 |
---|---|---|---|---|---|---|---|---|---|
nsv6290103 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 3,645,022 | 3,733,278 |
nsv6290103 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 3,684,654 | 3,772,910 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17955733 | copy number loss | Oligo aCGH | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17955733 | Remapped | Perfect | NC_000007.14:g.(?_ 3645022)_(3733278_ ?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 3,645,022 | 3,733,278 |
nssv17955733 | Submitted genomic | NC_000007.13:g.(?_ 3684654)_(3772910_ ?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 3,684,654 | 3,772,910 |