nsv3070140
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:929
- Data Source:HUMANGENOME_JCVI
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: 187 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 187 SVs from 46 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3070140 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 19,685,347 | 19,686,275 |
nsv3070140 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 19,685,578 | 19,686,506 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis |
---|---|---|---|---|
nssv14040833 | deletion | 1104685175673 | Curated | Curated |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14040833 | Remapped | Perfect | NC_000006.12:g.196 85347_19686275del9 29 | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 19,685,347 | 19,686,275 |
nssv14040833 | Submitted genomic | NC_000006.11:g.196 85578_19686506del9 29 | GRCh37 (hg19) | NC_000006.11 | Chr6 | 19,685,578 | 19,686,506 |