nsv4440823
- Organism: Homo sapiens
- Study:nstd175 (Genome in a Bottle)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:73
- Description:SVTYPE=DEL;REPTYPE=SIMPLEDEL
- Publication(s):Genome in a Bottle
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: 158 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 158 SVs from 39 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4440823 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 37,361,798 | 37,361,870 |
nsv4440823 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 35,990,201 | 35,990,273 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15763378 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15763378 | Remapped | Perfect | NC_000020.11:g.373 61798_37361870del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 37,361,798 | 37,361,870 |
nssv15763378 | Submitted genomic | NC_000020.10:g.359 90201_35990273del | GRCh37 (hg19) | NC_000020.10 | Chr20 | 35,990,201 | 35,990,273 |