nsv6623612
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:59,816
- Publication(s):Zarrei et al. 2023
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: 1988 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1994 SVs from 93 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6623612 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 33,752,843 | 33,812,658 |
| nsv6623612 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 33,555,310 | 33,615,125 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18308981 | Remapped | Perfect | NC_000016.10:g.(?_ 33752843)_(3381265 8_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 33,752,843 | 33,812,658 |
| nssv18316668 | Remapped | Perfect | NC_000016.10:g.(?_ 33752843)_(3381265 8_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 33,752,843 | 33,812,658 |
| nssv18308981 | Submitted genomic | NC_000016.9:g.(?_3 3555310)_(33615125 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 33,555,310 | 33,615,125 | ||
| nssv18316668 | Submitted genomic | NC_000016.9:g.(?_3 3555310)_(33615125 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 33,555,310 | 33,615,125 |