nsv4743909
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:53,297
- Publication(s):Quan 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: 356 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 356 SVs from 62 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4743909 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 16,309,275 | 16,362,571 |
nsv4743909 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 16,348,900 | 16,402,196 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16270285 | deletion | Sequencing | Split read mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16270285 | Remapped | Perfect | NC_000007.14:g.163 09275_16362571del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 16,309,275 | 16,362,571 |
nssv16270285 | Submitted genomic | NC_000007.13:g.163 48900_16402196del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 16,348,900 | 16,402,196 |