nsv4541484
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):gnomAD_Structural_Variants
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: 40 SVs from 8 studies. See in: genome view
Overlapping variant regions from other studies: 40 SVs from 8 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4541484 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 102,523,620 | 102,523,620 |
nsv4541484 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000011.9 | Chr11 | 102,394,351 | 102,394,351 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15997411 | insertion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15997411 | Remapped | Perfect | NC_000011.10:g.102 523620_102523621in s317 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 102,523,620 | 102,523,620 |
nssv15997411 | Submitted genomic | NC_000011.9:g.1023 94351_102394352ins 317 | GRCh37.p13 | NC_000011.9 | Chr11 | 102,394,351 | 102,394,351 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
---|---|---|---|
nssv15997411 | <0.001 | 6 | 21694 |