nsv4423754
- Organism: Homo sapiens
- Study:nstd174 (DGV Gold Standard)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:83,370
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 297 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 297 SVs from 52 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4423754 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 21,473,577 | 21,473,577 | 21,556,946 | 21,556,946 |
nsv4423754 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 21,762,506 | 21,762,506 | 21,845,875 | 21,845,875 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15715137 | copy number loss | Multiple | Multiple |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15715137 | Remapped | Perfect | NC_000010.11:g.(21 473577_21473577)_( 21556946_21556946) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 21,473,577 | 21,473,577 | 21,556,946 | 21,556,946 |
nssv15715137 | Submitted genomic | NC_000010.10:g.(21 762506_21762506)_( 21845875_21845875) del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 21,762,506 | 21,762,506 | 21,845,875 | 21,845,875 |