nsv4375217
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:38,220
- 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: 478 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 478 SVs from 73 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 |
---|---|---|---|---|---|---|---|---|---|
nsv4375217 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 156,044,674 | 156,082,893 |
nsv4375217 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 155,471,684 | 155,509,903 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15613709 | Remapped | Perfect | NC_000005.10:g.(?_ 156044674)_(156082 893_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 156,044,674 | 156,082,893 |
nssv15667754 | Remapped | Perfect | NC_000005.10:g.(?_ 156044674)_(156082 893_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 156,044,674 | 156,082,893 |
nssv15613709 | Submitted genomic | NC_000005.9:g.(?_1 55471684)_(1555099 03_?)del | GRCh37 (hg19) | NC_000005.9 | Chr5 | 155,471,684 | 155,509,903 | ||
nssv15667754 | Submitted genomic | NC_000005.9:g.(?_1 55471684)_(1555099 03_?)del | GRCh37 (hg19) | NC_000005.9 | Chr5 | 155,471,684 | 155,509,903 |