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nsv831021

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:242,323

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 619 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):69,657,183-69,899,505Question Mark
Overlapping variant regions from other studies: 619 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):69,122,169-69,364,491Question Mark
Overlapping variant regions from other studies: 25 SVs from 3 studies. See in: genome view    
Submitted genomic68,566,820-68,809,142Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv831021RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr769,657,18369,899,505
nsv831021RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr769,122,16969,364,491
nsv831021Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000007.11Chr768,566,82068,809,142

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1446195copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1446195RemappedPerfectNC_000007.14:g.(69
657183_?)_(?_69899
505)del
GRCh38.p12First PassNC_000007.14Chr769,657,18369,899,505
nssv1446195RemappedPerfectNC_000007.13:g.(69
122169_?)_(?_69364
491)del
GRCh37.p13First PassNC_000007.13Chr769,122,16969,364,491
nssv1446195Submitted genomicNC_000007.11:g.(68
566820_?)_(?_68809
142)del
NCBI35 (hg17)NC_000007.11Chr768,566,82068,809,142

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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