nsv6131352
- Organism: Homo sapiens
- Study:nstd186 (NCBI Curated Common Structural Variants)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:34
- Description:nsv5545014 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.
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: 278 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 57 SVs from 14 studies. See in: genome view
Overlapping variant regions from other studies: 276 SVs from 31 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6131352 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 45,914,223 | 45,914,256 |
| nsv6131352 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_2 | Second Pass | NT_187663.1 | Chr17|NT_1 87663.1 | 616,338 | 616,371 |
| nsv6131352 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 43,991,589 | 43,991,622 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17966171 | insertion | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17966171 | Remapped | Perfect | NT_187663.1:g.6163 38_616371ins? | GRCh38.p12 | Second Pass | NT_187663.1 | Chr17|NT_1 87663.1 | 616,338 | 616,371 |
| nssv17966171 | Remapped | Perfect | NC_000017.11:g.459 14223_45914256ins? | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 45,914,223 | 45,914,256 |
| nssv17966171 | Submitted genomic | NC_000017.10:g.439 91589_43991622ins? | GRCh37 (hg19) | NC_000017.10 | Chr17 | 43,991,589 | 43,991,622 |
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) |
|---|---|---|---|
| nssv17966171 | 0.094 | 569 | 6074 |