nsv4262355
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:109
- 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: 60 SVs from 5 studies. See in: genome view
Overlapping variant regions from other studies: 60 SVs from 5 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4262355 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 47,172,221 | 47,172,329 |
nsv4262355 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000018.9 | Chr18 | 44,698,592 | 44,698,700 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15840650 | deletion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15840650 | Remapped | Perfect | NC_000018.10:g.471 72221_47172329del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 47,172,221 | 47,172,329 |
nssv15840650 | Submitted genomic | NC_000018.9:g.4469 8592_44698700del | GRCh37.p13 | NC_000018.9 | Chr18 | 44,698,592 | 44,698,700 |
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) |
---|---|---|---|
nssv15840650 | <0.001 | 7 | 21694 |