nsv4380296
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:155,752,212
- Publication(s):Zarrei 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: 236290 SVs from 124 studies. See in: genome view
Overlapping variant regions from other studies: 235448 SVs from 124 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 |
---|---|---|---|---|---|---|---|---|---|
nsv4380296 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 251,880 | 156,004,091 |
nsv4380296 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 168,547 | 155,233,756 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|
nssv15644333 | Remapped | Good | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 251,880 | 156,004,091 |
nssv15666924 | Remapped | Good | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 251,880 | 156,004,091 |
nssv15675000 | Remapped | Good | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 251,880 | 156,004,091 |
nssv15644333 | Submitted genomic | GRCh37 (hg19) | NC_000023.10 | ChrX | 168,547 | 155,233,756 | ||
nssv15666924 | Submitted genomic | GRCh37 (hg19) | NC_000023.10 | ChrX | 168,547 | 155,233,756 | ||
nssv15675000 | Submitted genomic | GRCh37 (hg19) | NC_000023.10 | ChrX | 168,547 | 155,233,756 |