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esv29961

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:159,768

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2535 SVs from 114 studies. See in: genome view    
Remapped(Score: Perfect):196,769,767-196,929,534Question Mark
Overlapping variant regions from other studies: 2535 SVs from 114 studies. See in: genome view    
Remapped(Score: Perfect):196,738,897-196,898,664Question Mark
Overlapping variant regions from other studies: 1272 SVs from 37 studies. See in: genome view    
Submitted genomic195,005,520-195,165,287Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv29961RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1196,769,767196,929,534
esv29961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1196,738,897196,898,664
esv29961Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1195,005,520195,165,287

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv84200copy number gainWATSONOligo aCGHProbe signal intensity23

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv84200RemappedPerfectNC_000001.11:g.(?_
196769767)_(196929
534_?)dup
GRCh38.p12First PassNC_000001.11Chr1196,769,767196,929,534
essv84200RemappedPerfectNC_000001.10:g.(?_
196738897)_(196898
664_?)dup
GRCh37.p13First PassNC_000001.10Chr1196,738,897196,898,664
essv84200Submitted genomicNC_000001.9:g.(?_1
95005520)_(1951652
87_?)dup
NCBI36 (hg18)NC_000001.9Chr1195,005,520195,165,287

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv842002WATSONOligo aCGHProbe signal intensityPass
essv842004WATSONOligo aCGHProbe signal intensityPass
essv842003WATSONSequencingRead depthPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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