nsv4375620
- 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:722,008
- 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: 5997 SVs from 121 studies. See in: genome view
Overlapping variant regions from other studies: 6032 SVs from 121 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 |
---|---|---|---|---|---|---|---|---|---|
nsv4375620 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 22,194,192 | 22,916,199 |
nsv4375620 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 22,548,592 | 23,258,369 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15640275 | Remapped | Good | NC_000022.11:g.(?_ 22194192)_(2291619 9_?)del | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 22,194,192 | 22,916,199 |
nssv15642490 | Remapped | Good | NC_000022.11:g.(?_ 22194192)_(2291619 9_?)del | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 22,194,192 | 22,916,199 |
nssv15640275 | Submitted genomic | NC_000022.10:g.(?_ 22548592)_(2325836 9_?)del | GRCh37 (hg19) | NC_000022.10 | Chr22 | 22,548,592 | 23,258,369 | ||
nssv15642490 | Submitted genomic | NC_000022.10:g.(?_ 22548592)_(2325836 9_?)del | GRCh37 (hg19) | NC_000022.10 | Chr22 | 22,548,592 | 23,258,369 |