nsv4360624
- 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:90,848
- 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: 501 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 501 SVs from 57 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4360624 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 72,996,088 | 73,005,239 | 73,077,790 | 73,086,935 |
nsv4360624 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 72,215,927 | 72,225,078 | 72,297,629 | 72,306,774 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15607158 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15607158 | Remapped | Perfect | NC_000023.11:g.(72 996088_73005239)_( 73077790_73086935) inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 72,996,088 | 73,005,239 | 73,077,790 | 73,086,935 |
nssv15607158 | Submitted genomic | NC_000023.10:g.(72 215927_72225078)_( 72297629_72306774) inv | GRCh37.p13 | NC_000023.10 | ChrX | 72,215,927 | 72,225,078 | 72,297,629 | 72,306,774 |