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nsv469821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,731

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1512 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):21,448,386-21,614,116Question Mark
Overlapping variant regions from other studies: 1541 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):21,448,495-21,614,225Question Mark
Overlapping variant regions from other studies: 3 SVs from 1 studies. See in: genome view    
Submitted genomic21,493,996-21,659,726Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469821RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr521,448,38621,614,116
nsv469821RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr521,448,49521,614,225
nsv469821Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000005.7Chr521,493,99621,659,726

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1674589copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1674589RemappedPerfectNC_000005.10:g.(?_
21448386)_(2161411
6_?)dup
GRCh38.p12First PassNC_000005.10Chr521,448,38621,614,116
nssv1674589RemappedPerfectNC_000005.9:g.(?_2
1448495)_(21614225
_?)dup
GRCh37.p13First PassNC_000005.9Chr521,448,49521,614,225
nssv1674589Submitted genomicNC_000005.7:g.(?_2
1493996)_(21659726
_?)dup
NCBI34 (hg16)NC_000005.7Chr521,493,99621,659,726

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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