nsv5697537
- Organism: Homo sapiens
- Study:nstd211 (Chuang et al. 2021)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Insertion of a Alu mobile element relative to the reference
- Publication(s):Chuang 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: 120 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 114 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 8 SVs from 6 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5697537 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000019.10 | Chr19 | 41,799,481 | 41,799,481 | ||
nsv5697537 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000019.9 | Chr19 | 42,303,413 | 42,303,413 |
nsv5697537 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004775434.1 | Chr19|NW_0 04775434.1 | 368,520 | 368,520 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17199858 | alu insertion | Sequencing | Other |
nssv17224618 | alu insertion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17199858 | Submitted genomic | NC_000019.10:g.417 99481_41799482ins2 80 | GRCh38 (hg38) | NC_000019.10 | Chr19 | 41,799,481 | 41,799,481 | ||
nssv17224618 | Submitted genomic | NC_000019.10:g.417 99481_41799482ins2 80 | GRCh38 (hg38) | NC_000019.10 | Chr19 | 41,799,481 | 41,799,481 | ||
nssv17199858 | Remapped | Perfect | NW_004775434.1:g.3 68520_368521ins280 | GRCh37.p13 | First Pass | NW_004775434.1 | Chr19|NW_0 04775434.1 | 368,520 | 368,520 |
nssv17224618 | Remapped | Perfect | NW_004775434.1:g.3 68520_368521ins280 | GRCh37.p13 | First Pass | NW_004775434.1 | Chr19|NW_0 04775434.1 | 368,520 | 368,520 |
nssv17199858 | Remapped | Perfect | NC_000019.9:g.4230 3413_42303414ins28 0 | GRCh37.p13 | Second Pass | NC_000019.9 | Chr19 | 42,303,413 | 42,303,413 |
nssv17224618 | Remapped | Perfect | NC_000019.9:g.4230 3413_42303414ins28 0 | GRCh37.p13 | Second Pass | NC_000019.9 | Chr19 | 42,303,413 | 42,303,413 |