nsv6290100
- 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:35,763
- 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: 190 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 190 SVs from 43 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 |
---|---|---|---|---|---|---|---|---|---|
nsv6290100 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 49,656,751 | 49,692,513 |
nsv6290100 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 49,624,464 | 49,660,226 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17955737 | copy number gain | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv17955737 | Remapped | Perfect | NC_000006.12:g.(?_ 49656751)_(4969251 3_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 49,656,751 | 49,692,513 |
nssv17955737 | Submitted genomic | NC_000006.11:g.(?_ 49624464)_(4966022 6_?)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 49,624,464 | 49,660,226 |