nsv4630725
- Organism: Homo sapiens
- Study:nstd183 (DECIPHER Consensus CNVs)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:608
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: 63 SVs from 13 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view
Overlapping variant regions from other studies: 64 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4630725 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | Second Pass | NC_000014.9 | Chr14 | 24,371,703 | 24,372,310 |
| nsv4630725 | Remapped | Perfect | GRCh38.p12 | PATCHES | First Pass | NW_018654722.1 | Chr14|NW_0 18654722.1 | 672,681 | 673,288 |
| nsv4630725 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 24,840,909 | 24,841,516 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16150795 | duplication | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16150795 | Remapped | Perfect | NW_018654722.1:g.( ?_672681)_(673288_ ?)dup | GRCh38.p12 | First Pass | NW_018654722.1 | Chr14|NW_0 18654722.1 | 672,681 | 673,288 |
| nssv16150795 | Remapped | Perfect | NC_000014.9:g.(?_2 4371703)_(24372310 _?)dup | GRCh38.p12 | Second Pass | NC_000014.9 | Chr14 | 24,371,703 | 24,372,310 |
| nssv16150795 | Submitted genomic | NC_000014.8:g.(?_2 4840909)_(24841516 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 24,840,909 | 24,841,516 |
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) |
|---|---|---|---|
| nssv16150795 | 0.001 | 1 | 845 |