nsv426234
- Organism: Homo sapiens
- Study:nstd6 (Mills et al. 2006)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Mills et al. 2006
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 404 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 405 SVs from 20 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv426234 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 18,900,912 | 18,900,912 |
nsv426234 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 21,062,798 | 21,062,798 |
nsv426234 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000024.7 | ChrY | 19,450,923 | 19,450,923 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv444812 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv444812 | Remapped | Perfect | NC_000024.10:g.189 00912_18900913insG T | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 18,900,912 | 18,900,912 |
nssv444812 | Remapped | Perfect | NC_000024.9:g.2106 2798_21062799insGT | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 21,062,798 | 21,062,798 |
nssv444812 | Submitted genomic | NC_000024.7:g.1945 0923_19450924insGT | NCBI35 (hg17) | NC_000024.7 | ChrY | 19,450,923 | 19,450,923 |