nsv4370561
- 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:88,820
- 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: 360 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 360 SVs from 55 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 |
---|---|---|---|---|---|---|---|---|---|
nsv4370561 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 21,212,780 | 21,301,599 |
nsv4370561 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 21,254,272 | 21,343,091 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15628885 | Remapped | Perfect | NC_000003.12:g.(?_ 21212780)_(2130159 9_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 21,212,780 | 21,301,599 |
nssv15666554 | Remapped | Perfect | NC_000003.12:g.(?_ 21212780)_(2130159 9_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 21,212,780 | 21,301,599 |
nssv15628885 | Submitted genomic | NC_000003.11:g.(?_ 21254272)_(2134309 1_?)dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 21,254,272 | 21,343,091 | ||
nssv15666554 | Submitted genomic | NC_000003.11:g.(?_ 21254272)_(2134309 1_?)dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 21,254,272 | 21,343,091 |