nsv4368627
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:199,921
- Publication(s):Zarrei et al. 2019
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: 823 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 823 SVs from 72 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4368627 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 75,517,995 | 75,717,915 |
| nsv4368627 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 73,514,076 | 73,713,995 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15637547 | Remapped | Good | NC_000017.11:g.(?_ 75517995)_(7571791 5_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 75,517,995 | 75,717,915 |
| nssv15637564 | Remapped | Good | NC_000017.11:g.(?_ 75517995)_(7571791 5_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 75,517,995 | 75,717,915 |
| nssv15637547 | Submitted genomic | NC_000017.10:g.(?_ 73514076)_(7371399 5_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 73,514,076 | 73,713,995 | ||
| nssv15637564 | Submitted genomic | NC_000017.10:g.(?_ 73514076)_(7371399 5_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 73,514,076 | 73,713,995 |