nsv3054722
- Organism: Homo sapiens
- Study:nstd140 (Fan et al. 2017)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,684
- Publication(s):Fan et al. 2017
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: 356 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 356 SVs from 59 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3054722 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 72,154,149 | 72,163,832 | ||
nsv3054722 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 72,863,852 | 72,873,535 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14021072 | Submitted genomic | NC_000006.12:g.721 54149_72163832del | GRCh38 (hg38) | NC_000006.12 | Chr6 | 72,154,149 | 72,163,832 | ||
nssv14021072 | Remapped | Perfect | NC_000006.11:g.728 63852_72873535del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 72,863,852 | 72,873,535 |