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nsv482393

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:140,785

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1073 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):21,458,097-21,598,881Question Mark
Overlapping variant regions from other studies: 1102 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):21,458,206-21,598,990Question Mark
Overlapping variant regions from other studies: 3 SVs from 1 studies. See in: genome view    
Submitted genomic21,503,707-21,644,491Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv482393RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr521,458,09721,598,881
nsv482393RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr521,458,20621,598,990
nsv482393Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000005.7Chr521,503,70721,644,491

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3007687copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3007687RemappedPerfectNC_000005.10:g.(?_
21458097)_(2159888
1_?)dup
GRCh38.p12First PassNC_000005.10Chr521,458,09721,598,881
nssv3007687RemappedPerfectNC_000005.9:g.(?_2
1458206)_(21598990
_?)dup
GRCh37.p13First PassNC_000005.9Chr521,458,20621,598,990
nssv3007687Submitted genomicNC_000005.7:g.(?_2
1503707)_(21644491
_?)dup
NCBI34 (hg16)NC_000005.7Chr521,503,70721,644,491

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

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