nsv4443863
- Organism: Homo sapiens
- Study:nstd175 (Genome in a Bottle)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:SVTYPE=INS;REPTYPE=SIMPLEINS
- Publication(s):Genome in a Bottle
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: 147 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 147 SVs from 28 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4443863 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 37,914,404 | 37,914,404 |
nsv4443863 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 36,542,806 | 36,542,806 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15763937 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15763937 | Remapped | Perfect | NC_000020.11:g.379 14404_37914405ins2 38 | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 37,914,404 | 37,914,404 |
nssv15763937 | Submitted genomic | NC_000020.10:g.365 42806_36542807ins2 38 | GRCh37 (hg19) | NC_000020.10 | Chr20 | 36,542,806 | 36,542,806 |