nsv4432103
- Organism: Homo sapiens
- Study:nstd172 (Deng et al. 2019)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:60,577
- Publication(s):Deng et al. 2019
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: 677 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 677 SVs from 76 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4432103 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 41,139,885 | 41,200,461 |
nsv4432103 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000014.8 | Chr14 | 41,609,088 | 41,669,664 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv15752670 | deletion | NB11 | Sequencing | Sequence alignment | 596 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15752670 | Remapped | Perfect | NC_000014.9:g.4113 9885_41200461del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 41,139,885 | 41,200,461 |
nssv15752670 | Submitted genomic | NC_000014.8:g.4160 9088_41669664del | GRCh37.p13 | NC_000014.8 | Chr14 | 41,609,088 | 41,669,664 |