nsv398013
- Organism: Homo sapiens
- Study:nstd6 (Mills et al. 2006)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,925
- 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: 218 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 218 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 5 SVs from 1 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv398013 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 32,474,675 | 32,484,599 |
nsv398013 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 32,332,191 | 32,342,115 |
nsv398013 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 32,451,733 | 32,461,657 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv416591 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv416591 | Remapped | Perfect | NC_000008.11:g.324 74675_32484599del9 925 | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 32,474,675 | 32,484,599 |
nssv416591 | Remapped | Perfect | NC_000008.10:g.323 32191_32342115del9 925 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 32,332,191 | 32,342,115 |
nssv416591 | Submitted genomic | NC_000008.9:g.3245 1733_32461657del99 25 | NCBI35 (hg17) | NC_000008.9 | Chr8 | 32,451,733 | 32,461,657 |