nsv4360636
- Organism: Homo sapiens
- Study:nstd169 (Giner-Delgado et al. 2019)
- Variant Type:inversion
- Method Type:MLPA
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:52,607
- Publication(s):Giner-Delgado et al. 2019
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: 736 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 736 SVs from 78 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360636 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 63,716,851 | 63,721,108 | 63,765,200 | 63,769,457 |
| nsv4360636 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000013.10 | Chr13 | 64,290,984 | 64,295,241 | 64,339,333 | 64,343,590 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607146 | inversion | MLPA | Genotyping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607146 | Remapped | Perfect | NC_000013.11:g.(63 716851_63721108)_( 63765200_63769457) inv | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 63,716,851 | 63,721,108 | 63,765,200 | 63,769,457 |
| nssv15607146 | Submitted genomic | NC_000013.10:g.(64 290984_64295241)_( 64339333_64343590) inv | GRCh37.p13 | NC_000013.10 | Chr13 | 64,290,984 | 64,295,241 | 64,339,333 | 64,343,590 |