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esv16507

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:72,027

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 477 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):55,459,713-55,531,739Question Mark
Overlapping variant regions from other studies: 477 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):57,219,473-57,291,499Question Mark
Overlapping variant regions from other studies: 125 SVs from 24 studies. See in: genome view    
Submitted genomic56,889,479-56,961,505Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv16507RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1055,459,71355,531,739
esv16507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1057,219,47357,291,499
esv16507Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1056,889,47956,961,505

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv73657copy number lossNA12156Oligo aCGHProbe signal intensity1,085

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv73657RemappedPerfectNC_000010.11:g.(?_
55459713)_(5553173
9_?)del
GRCh38.p12First PassNC_000010.11Chr1055,459,71355,531,739
essv73657RemappedPerfectNC_000010.10:g.(?_
57219473)_(5729149
9_?)del
GRCh37.p13First PassNC_000010.10Chr1057,219,47357,291,499
essv73657Submitted genomicNC_000010.9:g.(?_5
6889479)_(56961505
_?)del
NCBI36 (hg18)NC_000010.9Chr1056,889,47956,961,505

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv736572NA12156Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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