nsv4661560
- Organism: Homo sapiens
- Study:nstd186 (NCBI Curated Common Structural Variants)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:41,891
- Description:nsv4605814 from DECIPHER Consensus CNVs. For a full list of variants now included in nstd186, refer to the mapping file provided here.
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: 556 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 556 SVs from 60 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4661560 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 152,205,725 | 152,247,615 |
| nsv4661560 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 151,902,810 | 151,944,700 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16199847 | duplication | Curated | Curated |
| nssv16203030 | deletion | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16199847 | Remapped | Perfect | NC_000007.14:g.(?_ 152205725)_(152247 615_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 152,205,725 | 152,247,615 |
| nssv16203030 | Remapped | Perfect | NC_000007.14:g.(?_ 152205725)_(152247 615_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 152,205,725 | 152,247,615 |
| nssv16199847 | Submitted genomic | NC_000007.13:g.(?_ 151902810)_(151944 700_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 151,902,810 | 151,944,700 | ||
| nssv16203030 | Submitted genomic | NC_000007.13:g.(?_ 151902810)_(151944 700_?)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 151,902,810 | 151,944,700 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16199847 | 0.026 | 22 | 845 |
| nssv16203030 | 0.011 | 9 | 845 |