nsv4417741
- Organism: Homo sapiens
- Study:nstd174 (DGV Gold Standard)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:186,832
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 870 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 871 SVs from 92 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4417741 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 20,043,514 | 20,043,514 | 20,230,345 | 20,230,345 |
| nsv4417741 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 20,511,673 | 20,511,673 | 20,698,504 | 20,698,504 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15721293 | copy number loss | Multiple | Multiple |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15721293 | Remapped | Perfect | NC_000014.9:g.(200 43514_20043514)_(2 0230345_20230345)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 20,043,514 | 20,043,514 | 20,230,345 | 20,230,345 |
| nssv15721293 | Submitted genomic | NC_000014.8:g.(205 11673_20511673)_(2 0698504_20698504)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 20,511,673 | 20,511,673 | 20,698,504 | 20,698,504 |