nsv5975558
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Almarri et al. 2020
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: 244 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 24 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5975558 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 102,783,563 | 102,783,563 | ||
nsv5975558 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 103,435,913 | 103,435,913 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17360004 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17360004 | Submitted genomic | NC_000013.11:g.102 783563_102783564in s125 | GRCh38 (hg38) | NC_000013.11 | Chr13 | 102,783,563 | 102,783,563 | ||
nssv17360004 | Remapped | Perfect | NC_000013.10:g.103 435913_103435914in s125 | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 103,435,913 | 103,435,913 |