nsv6350919
- Organism: Homo sapiens
- Study:nstd223 (Sedlazeck et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,760,682
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: 5527 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 5533 SVs from 91 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6350919 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 146,838,349 | 149,599,030 | ||
nsv6350919 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 147,595,917 | 150,455,544 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18205489 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18205489 | Submitted genomic | NC_000002.12:g.146 838349_149599030du p | GRCh38 (hg38) | NC_000002.12 | Chr2 | 146,838,349 | 149,599,030 | ||
nssv18205489 | Remapped | Good | NC_000002.11:g.147 595917_150455544du p | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 147,595,917 | 150,455,544 |
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) |
---|---|---|---|
nssv18205489 | <0.001 | 4 | 36086 |