nsv6631800
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:86,507
- 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: 366 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 366 SVs from 55 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 |
---|---|---|---|---|---|---|---|---|---|
nsv6631800 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 101,539,827 | 101,626,333 |
nsv6631800 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 101,183,108 | 101,269,613 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv18312951 | duplication | OSC7685 | SNP array | Probe signal intensity | 12 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18312951 | Remapped | Good | NC_000007.14:g.(?_ 101539827)_(101626 333_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 101,539,827 | 101,626,333 |
nssv18312951 | Submitted genomic | NC_000007.13:g.(?_ 101183108)_(101269 613_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 101,183,108 | 101,269,613 |