nsv4614592
- Organism: Homo sapiens
- Study:nstd183 (DECIPHER Consensus CNVs)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:571,335
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: 4369 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 4368 SVs from 93 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4614592 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 37,486,302 | 38,057,636 |
| nsv4614592 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 37,880,104 | 38,451,438 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16136766 | deletion | Curated | Curated |
| nssv16139184 | duplication | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16136766 | Remapped | Perfect | NC_000012.12:g.(?_ 37486302)_(3805763 6_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 37,486,302 | 38,057,636 |
| nssv16139184 | Remapped | Perfect | NC_000012.12:g.(?_ 37486302)_(3805763 6_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 37,486,302 | 38,057,636 |
| nssv16136766 | Submitted genomic | NC_000012.11:g.(?_ 37880104)_(3845143 8_?)del | GRCh37 (hg19) | NC_000012.11 | Chr12 | 37,880,104 | 38,451,438 | ||
| nssv16139184 | Submitted genomic | NC_000012.11:g.(?_ 37880104)_(3845143 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 37,880,104 | 38,451,438 |
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) |
|---|---|---|---|
| nssv16136766 | <0.001 | 2 | 5919 |
| nssv16139184 | <0.001 | 4 | 5919 |