nsv4034377
- 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:519,829
- 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: 542 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 543 SVs from 19 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4034377 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 4,593,415 | 5,113,243 |
nsv4034377 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 4,511,456 | 5,031,284 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15987767 | duplication | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15987767 | Remapped | Perfect | NC_000023.11:g.459 3415_5113243dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 4,593,415 | 5,113,243 |
nssv15987767 | Submitted genomic | NC_000023.10:g.451 1456_5031284dup | GRCh37.p13 | NC_000023.10 | ChrX | 4,511,456 | 5,031,284 |
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) |
---|---|---|---|
nssv15987767 | <0.001 | 4 | 21036 |