nsv4849088
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:780
- 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: 164 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 164 SVs from 33 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4849088 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 90,316,906 | 90,317,685 |
| nsv4849088 | Remapped | Perfect | GRCh38.p12 | PATCHES | Second Pass | NW_019805497.1 | Chr11|NW_0 19805497.1 | 253,840 | 254,619 |
| nsv4849088 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 90,050,074 | 90,050,853 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16337301 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16337301 | Remapped | Perfect | NW_019805497.1:g.2 53840_254619del | GRCh38.p12 | Second Pass | NW_019805497.1 | Chr11|NW_0 19805497.1 | 253,840 | 254,619 |
| nssv16337301 | Remapped | Perfect | NC_000011.10:g.903 16906_90317685del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 90,316,906 | 90,317,685 |
| nssv16337301 | Submitted genomic | NC_000011.9:g.9005 0074_90050853del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 90,050,074 | 90,050,853 |
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) |
|---|---|---|---|
| nssv16337301 | <0.001 | 1 | 16834 |