nsv4985096
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:279,750
- Publication(s):Abel et al. 2020
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: 1044 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1040 SVs from 96 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4985096 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 67,713,933 (-215, +1) | 67,993,682 (-2, +123) | ||
| nsv4985096 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 67,481,404 (-215, +1) | 67,761,153 (-2, +123) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16535621 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16535621 | Submitted genomic | NC_000011.10:g.(67 713718_67713934)_( 67993680_67993805) dup | GRCh38 (hg38) | NC_000011.10 | Chr11 | 67,713,933 (-215, +1) | 67,993,682 (-2, +123) | ||
| nssv16535621 | Remapped | Perfect | NC_000011.9:g.(674 81189_67481405)_(6 7761151_67761276)d up | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,481,404 (-215, +1) | 67,761,153 (-2, +123) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16535621 | <0.001 | 1 | 29246 |