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esv20105

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:107,993

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 577 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):54,179,969-54,287,961Question Mark
Overlapping variant regions from other studies: 577 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):55,939,729-56,047,721Question Mark
Overlapping variant regions from other studies: 192 SVs from 23 studies. See in: genome view    
Submitted genomic55,609,735-55,717,727Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv20105RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1054,179,96954,287,961
esv20105RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1055,939,72956,047,721
esv20105Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1055,609,73555,717,727

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv82599copy number lossNA19190Oligo aCGHProbe signal intensity1,600

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv82599RemappedPerfectNC_000010.11:g.(?_
54179969)_(5428796
1_?)del
GRCh38.p12First PassNC_000010.11Chr1054,179,96954,287,961
essv82599RemappedPerfectNC_000010.10:g.(?_
55939729)_(5604772
1_?)del
GRCh37.p13First PassNC_000010.10Chr1055,939,72956,047,721
essv82599Submitted genomicNC_000010.9:g.(?_5
5609735)_(55717727
_?)del
NCBI36 (hg18)NC_000010.9Chr1055,609,73555,717,727

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv825992NA19190Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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