nsv432366
- Organism: Homo sapiens
- Study:nstd12 (Marshall et al. 2008)
- Variant Type:copy number variation
- Method Type:Merging, SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:361,360
- Publication(s):Marshall et al. 2008
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: 1110 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 883 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 44 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 | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv432366 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 144,250,928 | 144,612,287 |
nsv432366 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 143,366,681 | 143,615,265 |
nsv432366 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 143,059,574 | 143,399,300 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv565727 | copy number gain | 79449 | Merging, SNP array | Merging, SNP genotyping analysis | 6 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv565727 | Remapped | Pass | NC_000023.11:g.(?_ 144250928)_(144612 287_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 144,250,928 | 144,612,287 |
nssv565727 | Remapped | Pass | NC_000023.10:g.(?_ 143366681)_(143615 265_?)dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 143,366,681 | 143,615,265 |
nssv565727 | Submitted genomic | NC_000023.8:g.(?_1 43059574)_(1433993 00_?)dup | NCBI35 (hg17) | NC_000023.8 | ChrX | 143,059,574 | 143,399,300 |