nsv3067177
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:delins
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,301
- 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: 235 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 235 SVs from 44 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3067177 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 55,850,249 | 55,851,549 |
nsv3067177 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 56,361,615 | 56,362,915 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis |
---|---|---|---|---|
nssv14042532 | delins | 1104685154615 | Curated | Curated |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14042532 | Remapped | Perfect | NC_000019.10:g.558 50249_55851549deli ns1281 | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 55,850,249 | 55,851,549 |
nssv14042532 | Submitted genomic | NC_000019.9:g.5636 1615_56362915delin s1281 | GRCh37 (hg19) | NC_000019.9 | Chr19 | 56,361,615 | 56,362,915 |