nsv3067502
- 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:1,456
- 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: 264 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 264 SVs from 42 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3067502 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 1,107,553 | 1,109,008 |
nsv3067502 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 1,103,239 | 1,104,694 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis |
---|---|---|---|---|
nssv14041983 | delins | 1104685353464 | Curated | Curated |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14041983 | Remapped | Perfect | NC_000002.12:g.110 7553_1109008delins 1716 | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,107,553 | 1,109,008 |
nssv14041983 | Submitted genomic | NC_000002.11:g.110 3239_1104694delins 1716 | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,103,239 | 1,104,694 |