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esv9999

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:53,848

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 563 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):189,015,146-189,068,993Question Mark
Overlapping variant regions from other studies: 563 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):188,984,277-189,038,124Question Mark
Overlapping variant regions from other studies: 205 SVs from 25 studies. See in: genome view    
Submitted genomic187,250,900-187,304,747Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv9999RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1189,015,146189,068,993
esv9999RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1188,984,277189,038,124
esv9999Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1187,250,900187,304,747

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv35542copy number lossNA18907Oligo aCGHProbe signal intensity1,412

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv35542RemappedPerfectNC_000001.11:g.(?_
189015146)_(189068
993_?)del
GRCh38.p12First PassNC_000001.11Chr1189,015,146189,068,993
essv35542RemappedPerfectNC_000001.10:g.(?_
188984277)_(189038
124_?)del
GRCh37.p13First PassNC_000001.10Chr1188,984,277189,038,124
essv35542Submitted genomicNC_000001.9:g.(?_1
87250900)_(1873047
47_?)del
NCBI36 (hg18)NC_000001.9Chr1187,250,900187,304,747

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv355422NA18907Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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