nsv1163551
- Organism: Homo sapiens
- Study:nstd109 (Wildschutte et al. 2015)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Wildschutte et al. 2015
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: 128 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 29 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv1163551 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 93,609,091 | 93,609,091 |
nsv1163551 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 96,371,373 | 96,371,373 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv4042639 | alu insertion | Sequencing | de novo and local sequence assembly |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv4042639 | Remapped | Perfect | NC_000009.12:g.936 09091_93609092ins3 32 | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 93,609,091 | 93,609,091 |
nssv4042639 | Submitted genomic | NC_000009.11:g.963 71373_96371374ins3 32 | GRCh37 (hg19) | NC_000009.11 | Chr9 | 96,371,373 | 96,371,373 |