nsv5602976
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:46,726
- Publication(s):Ebert et al. 2021
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: 393 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 393 SVs from 64 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5602976 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 55,190,250 | 55,236,975 | ||
nsv5602976 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 56,950,010 | 56,996,735 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17070730 | Submitted genomic | NC_000010.11:g.551 90250_55236975delG | GRCh38 (hg38) | NC_000010.11 | Chr10 | 55,190,250 | 55,236,975 | ||
nssv17070730 | Remapped | Perfect | NC_000010.10:g.569 50010_56996735delG | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 56,950,010 | 56,996,735 |