nsv4369708
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:167,146
- 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: 911 SVs from 87 studies. See in: genome view
Overlapping variant regions from other studies: 1081 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 1517 SVs from 102 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 |
---|---|---|---|---|---|---|---|---|---|
nsv4369708 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 142,618,685 | 142,785,830 |
nsv4369708 | Remapped | Pass | GRCh38.p12 | ALT_REF_LOCI_1 | First Pass | NT_187562.1 | Chr7|NT_18 7562.1 | 656,734 | 781,128 |
nsv4369708 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 142,246,905 | 142,493,639 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv15680703 | copy number gain | 215271 | SNP array | Genotyping | 21 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15680703 | Remapped | Pass | NT_187562.1:g.(?_6 56734)_(781128_?)d up | GRCh38.p12 | First Pass | NT_187562.1 | Chr7|NT_18 7562.1 | 656,734 | 781,128 |
nssv15680703 | Remapped | Pass | NC_000007.14:g.(?_ 142618685)_(142785 830_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 142,618,685 | 142,785,830 |
nssv15680703 | Submitted genomic | NC_000007.13:g.(?_ 142246905)_(142493 639_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 142,246,905 | 142,493,639 |