nsv4735399
- 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:51,268
- 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: 282 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 201 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 |
---|---|---|---|---|---|---|---|---|---|
nsv4735399 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 79,499,110 | 79,550,377 |
nsv4735399 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 77,495,192 | 77,596,461 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16290452 | deletion | Sequencing | Split read mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16290452 | Remapped | Pass | NC_000017.11:g.794 99110_79550377del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 79,499,110 | 79,550,377 |
nssv16290452 | Submitted genomic | NC_000017.10:g.774 95192_77596461del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 77,495,192 | 77,596,461 |