U.S. flag

An official website of the United States government

nsv590209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,571

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):46,976,724-47,009,294Question Mark
Overlapping variant regions from other studies: 162 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):47,018,214-47,050,784Question Mark
Overlapping variant regions from other studies: 43 SVs from 14 studies. See in: genome view    
Submitted genomic46,993,218-47,025,788Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv590209RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr346,976,72447,009,294
nsv590209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr347,018,21447,050,784
nsv590209Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr346,993,21847,025,788

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv962609copy number lossSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv962609RemappedPerfectNC_000003.12:g.(?_
46976724)_(4700929
4_?)del
GRCh38.p12First PassNC_000003.12Chr346,976,72447,009,294
nssv962609RemappedPerfectNC_000003.11:g.(?_
47018214)_(4705078
4_?)del
GRCh37.p13First PassNC_000003.11Chr347,018,21447,050,784
nssv962609Submitted genomicNC_000003.10:g.(?_
46993218)_(4702578
8_?)del
NCBI36 (hg18)NC_000003.10Chr346,993,21847,025,788

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center