nsv6112652
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Wu 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: 431 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 431 SVs from 43 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6112652 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000021.9 | Chr21 | 45,987,768 | 45,987,768 | ||
nsv6112652 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 47,407,682 | 47,407,682 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17641091 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17641091 | Submitted genomic | NC_000021.9:g.4598 7768_45987769ins65 | GRCh38 (hg38) | NC_000021.9 | Chr21 | 45,987,768 | 45,987,768 | ||
nssv17641091 | Remapped | Perfect | NC_000021.8:g.4740 7682_47407683ins65 | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 47,407,682 | 47,407,682 |