nsv930481
- Organism: Homo sapiens
- Study:nstd78 (Schrider et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Fail
- Clinical Assertions: No
- Region Size:655
- Description:A processed transcript of the RPL29 gene was reverse transcribed and reinserted into the genome. Since the insertion was detected in the reference assembly but not in a test sample, by convention it must be referred to here as a deletion.
- Publication(s):Schrider et al. 2013
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: 137 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 23 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv930481 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 117,998,928 | 117,999,582 |
nsv930481 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 118,320,091 | 118,320,745 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv1607672 | deletion | Sequencing | Paired-end mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1607672 | Remapped | Perfect | NC_000006.12:g.(11 7998928_?)_(?_1179 99582)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 117,998,928 | 117,999,582 |
nssv1607672 | Submitted genomic | NC_000006.11:g.(11 8320091_?)_(?_1183 20745)del640 | GRCh37 (hg19) | NC_000006.11 | Chr6 | 118,320,091 | 118,320,745 |
Validation Information
Variant Call ID | Experiment ID | Method | Analysis | Result |
---|---|---|---|---|
nssv1607672 | 2 | PCR | Manual observation | Fail |