nsv2800976
- Organism: Homo sapiens
- Study:nstd137 (Huddleston et al. 2016)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:18,553
- Publication(s):Huddleston et al. 2016
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: 296 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 302 SVs from 60 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv2800976 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 207,538,097 | 207,556,649 | ||
nsv2800976 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 207,711,442 | 207,729,994 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv13678816 | deletion | Sequencing | Genotyping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv13678816 | Submitted genomic | NC_000001.11:g.207 538097_207556649de l18553 | GRCh38 (hg38) | NC_000001.11 | Chr1 | 207,538,097 | 207,556,649 | ||
nssv13678816 | Remapped | Perfect | NC_000001.10:g.207 711442_207729994de l18553 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 207,711,442 | 207,729,994 |
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) |
---|---|---|---|
nssv13678816 | 0.778 | 42 | 54 |